SGID Silkworm Genome Informatics Database
Gene
KWMTBOMO08068  Validated by peptides from experiments
Pre Gene Modal
BGIBMGA014545
Annotation
PREDICTED:_cubilin-like_[Bombyx_mori]
Full name
Cubilin homolog       + More
Cubilin      
Probable cubilin      
Tolloid-like protein 2      
Tolloid-like protein 1      
Dorsal-ventral patterning tolloid-like protein 1      
Bone morphogenetic protein 1      
Deleted in malignant brain tumors 1 protein      
Dorsal-ventral patterning protein tolloid      
Neurogenic locus notch homolog protein 1      
Neurogenic locus notch homolog protein 4      
Neurogenic locus notch homolog protein 2      
Protein lin-12      
Neurogenic locus notch homolog protein 3      
Protein eyes shut homolog      
Protein jagged-1b      
Protein jagged-1a      
Fibropellin-1      
Protein crumbs homolog 2      
Protein jagged-1      
Neurogenic locus Notch protein      
Protein jagged-2      
Protein glp-1      
Sushi, nidogen and EGF-like domain-containing protein 1      
Protein crumbs      
Protein serrate      
Delta-like protein 1      
Protein crumbs homolog 1      
Growth arrest-specific protein 6      
Delta-like protein A      
Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1      
Delta-like protein D      
Delta-like protein C      
Neurogenic locus protein delta      
Stabilin-1      
Stabilin-2      
Thrombospondin-4      
Alternative Name
460 kDa receptor
Glycoprotein 280
Intrinsic factor-cobalamin receptor
Intrinsic factor-vitamin B12 receptor
Intestinal intrinsic factor receptor
Metalloprotease xolloid
Xenopus tolloid
Metalloprotease xolloid-like
Xenopus tolloid-like protein 1
Xlr
Chicken tolloid-like protein 1
Metalloprotease colloid
Mini fin protein
Mammalian tolloid protein
Procollagen C-proteinase
Apactin
CRP-ductin
Glycoprotein 300
Hensin
Mucin-like glycoprotein
Vomeroglandin
p80
Motch A
mT14
p300
Translocation-associated notch protein TAN-1
Abnormal cell lineage protein 12
Motch B
Epidermal growth factor-like protein 10
Epidermal growth factor-like protein 11
Protein spacemaker homolog
Jagged3
Epidermal growth factor-related protein 1
Fibropellin-I
SpEGF I
UEGF-1
Crumbs-like protein 2
Insulin-responsive sequence DNA-binding protein 1
Secreted protein SST-3
Stromal nidogen extracellular matrix protein
95F
Protein beaded
Drosophila Delta homolog 1
AXL receptor tyrosine kinase ligand
After eight protein
Fasciclin, EGF-like, laminin-type EGF-like and link domain-containing scavenger receptor 1
MS-1 antigen
CCP module-containing protein 22
Polydom
Selectin-like osteoblast-derived protein
Serologically defined breast cancer antigen NY-BR-38
Fasciclin, EGF-like, laminin-type EGF-like and link domain-containing scavenger receptor 2
Location in the cell
PlasmaMembrane   Reliability : 2.164
 

Sequence

CDS
ATGAACAGAAAATTAATCAATCTGCAACGAGAATTAGCACTGTTACGCGTGGATCAATGTCGCTTACAACCTTGCATGCATGGAGGAATATGTTTGAGCATATTAGATGGTTATCACTGCCTTTGCCCATCAAACTGGGAAGGACAAAATTGTGATATTGACGTCAACGAATGTCATAACTTTGCTGGTACAGACCTTGGTTGTCAGAATGGCGCAACTTGTATTAACAGACCAGGTTCATATGAATGTCTTTGTAAATCTGGCTGGTATGGCTTACATTGCACTAGAAAAGCTAAAGATTGTTCTGGAGGAGACTTCGAAATGTGTGGTCACGGTACGTGTGTTCCAGTTACAACAGGTCAAGGCGTTAAATGTATTTGTGACCAAGGCTGGACTACAAATGGAACCGATTTTTCTTGTCTCACGGATGTAAATGAATGTGAAGCAAGTCAGGGTCCCAGATGTTCAGTGAATCCAAAAGTAGAATGTATTAACTTACCAGGCTCATTTCGCTGTGGACAATGTCCACCTGGCTATCAGGGAGATGGTTACAGTTGTTCTGATATCGACGAATGTAGTACTATACCAAACGGAGGCTGCAGTCCAGTCGCAGCATGCCACAACACAATCGGATCGCGAATATGCGGCCCTTGTCCGCTTGGCTTCCAAGGCGACGGTGTTTCATGTTCTTGGAAAGGATCTTGCAACCTCGACCACGGAGGCTGCCATCCTTCTGCACAGTGCATCGACAATGGAAGAATGGGCGGTGCGGGCGCGCAGTGCATATGCCCCGAAGGAATGGAAGGTGATGGTTACGGTCTCAATGGCTGTTTTATCTCGAATGGAGGAAATCAAAGCTGCGCAAGTAGACCCTGTGGACTCAATGGGCGATGCCACACGTTACGTACAGGATACACTTGCGTTTGTCGTAAAGGTTTCAGTGGAGCTCATTGTGAAGTGCCAAGTAACTTATGCGCAAACAATCCATGTCTCAACGGAGGGGTATGTAGACTAGACGACCAAAATCCCAGAGGCTTTAGGTGTGAATGCACAGCACAGTATTCCGGACCAATTTGTCAACTAGTGTCCAAACGATGCGGCGGGGTACTTGATAATAACGAAGGTACTATTTCATATCCTGTTGCAAACACAACATACAACAATAACGCACGATGTGCATGGGTAATTCATACAAATCCGGATAAAGTAATTAACGTAACATTTACCAAATTTTATTTAGAATCTCATCCTGATTGTTTGTATGACTTTCTGCAAATACACGACGGACGAAGCTCTGCCAGTCAACTTTTAGGTAGATTTTGTGGTAACGAATTCCCTAAGGGCGGTAATATAATATCAAGCCATAACAATTTATATTTATGGTTTTCGTCTGACGCTACTGTAGCCAAAAATGGATTTACACTTCATTGGATTAGTGTGAAACCGATTTGTGGAGGCGATGTAGATGTTACGAAACATGGACAAATAAGTTCTCCTGGTTCACCAGGAAAATATCCCCCTAACCGCGACTGCTACTGGCACTTATCGACTACGTTAGAGAGACCCATAGCTCACAAGTGTACTCTCGGAGATTATTTAGAACTGAGGAATGGAGTTACAGAAAATTCACCAATCATAGATCAATTATGCGGCAACTTTGAGAAAAGAATAATTCTGTCCATGGCGAACGCTTTATATATTCGTTTCCATTCTGATTTTTATCTTTCTGGTAAAGGATTCAAATTAGAATGGGATGGAACCGTCATTGGATGTGGTGGCACTGTTACTAGTTCTAAAGGATCTATAGCTTCTCCAAACTATCCTAACAATTACCACGACTTCCAAGAGTGCTTTTATAAAATTGTTGCTAGCCCAGGTTCAAGAATTCATATTTCGTTTGTAGAGCTAGATCTCGAACGGACTCACGAGTGTGAAGACGATTACATTGAAATATACGACGGTCTTGATTCTAGCGCTAATAAGTTAGGACGATTTTGTACAATGTCCCCTGAATTAGTAAACATCGCAACTTCTTCCAATAGTGCATATTTAAAGTTTCGTTCTGACTTTTACCTAAGTGGTAAAGGATTTTTATTGAATTATGAAGCCGCCTGTCATAATAATATCACTGGAAATTACGGAGTTATAGAAACGCCAAATTTTCCCGGTTTCTATCCAGCTAATTCTAATTGTCTGTGGAATATAACCGTATCGAAAGGAAATCGGATAAATGTTACTTTCACGGATTTCAATCTATATAAACCCTACCGAGGTTATCCTTTTTCACGTTTAAATACGTTCTACAGATACCAAACTTGTCAGCATGATTACATACAAATTAAGGACTCAGCTGATTCAACTTTCTCCGATAAAATCTGTGGAAATAAAATACCTTCAATGATAACTACTAAAGAGAACTCGCTACAAATTAAATTTTTTTCTGGATACGTTCCGCGAACCGGCTTCCGTCTCGAATGGGTTAGATTTGGATGCGGTGGTGTTGTTCGTGCATCAAACGGAATTTTAGAACTGGAAAAACGTTTCATGTCGAGTAAAGAATTGGAATGTGAATGGACTATAAGAACTTCCATCGGGAAATCATTAATTTTAAACTTTAGCGACATTTACTTATCGGAGACTAAAGATTGTACAGAAGATGCTATAGAAGTGTATAACGGTGAAGATACTACATCGCCACTATTAACCAAAATATGCAGTCGAAAACCAACGTCCGTGCAATCTACAGCCAACGTTATGTTTGTAAGATTAAGCAAGCTCTCATCTCTCAAAGATGTTTATTTTAAATCCAAATATCGTTCTATAGCATCGACGTGCGGTGGCTCAATAAAATCTACTTCAGGATTTATTTATTCTAAAAACTACCCCAAGAATTACGATAACAATTTAGATTGTTTATGGAAGATTGAAGTAGCCAAGGATCATCGAATTGCATTGAATTTTACAGACGTAGATTTATACTCCGAAAACGTTGCTCCTGGCCATGATTGTAACGACCGAATCGAAGTATACGATAATATGTTTAATATGCTTACAAAAACATACAAATATCATATCTGTTCTCGGTCCGATACAAAATCTTTTGTCAGTGATTCAAACACGATTTACGTTAAATTTGTTACTGATAACGTAGGAACAGCTAAAGGATTTAAAGGCAATTTTAATACTGTTTGCGGAAGCTCTATTACCGCCATCACCGACGGAACTATTTCAAGCGATAAACACCCGTATTCGAATAGCTGCAGCTGGACAATTAAAGCATCAGATTTAGATAAAAAAATATCGTTATCATTAACTCATATAGCACTACCAACCGATTTTAGTAATTTTATTAATAGAACCTGCTCTTCGACATACCTTCGTCTATACGATGGGGATGACACTAATGCGCCGGAGATAGGAGAATACTGCGGACGAAAAATACCTCCACTAATAGTAAGTCATGGAAGCGCTATCACCATGGAACTGGGGACGTACAGTAATAAAATTGAAGGGGAATTTTCTGCACACTATTCGACGTTATCTAATGCATGTGGAGGAACGTACACTTCCGAAGAGGGAGCACTAGCATCACCGAACTATCCCCGCCCTTACCCATCAGGCGTTGATTGTGAATGGATAATAAAAGCATCGCCTGGTAATCAGATATACATCACATTCGAAAGTTTTAATTTAGAATTTTCTGAAGCATGTAATGAGGATTATTTAGAATTACGTGAAAATTCTGGTAGCGGACAATTACTTGATGTATACTGTGGCAATGATATTCCATCAAATGTTACAATTGGAAATAAATTGTACATCAAATTTCACAGTAAAATGCAAAGTACTGTGAAAACTAATGGTTTCCTTATTCATTATGGATTACTGCATAATAATGAAATCACAGGTGATCATGGAAGAATTACGTCACCGCTGTATCCAAATCTTTACCACGATTCTGGTGATTTCACTTGGCGAATAATCACAACCGCACGTAAAACTATTTCAATAAAATTTGACACCTTGAACATTCCAACGTATGGTGATATTTGTTTTAACAAGCTAAGTATTTACGATGGATATGATAGTTCGGGACGCCTTTTAACAGAACTTTGTGGAGTAACCCTTGAATCGGACACATTTGAAACATCCTCAAATGCCATTTTCATTAAATTTTCCCTGGACGGATCTAACACAGGATCACTATTTAGTTTAACGTGGACAAGTTCCGATAAAATAATGATCAATGAAGATGAAAATGAAATCATTAATTGCGGATCTAACGAAACGCAAACATTGTTACCTGGTGAGATTAAGATAATTAAATCGCCAAATTATCCAAATCCGTATGACATTGATCTAAACTGTAAATGGGAATTCAAAGGTACTTTAGGAAATCATCTTAAGATCTCTTTTATAGATTTTAACTTAGAAGAAACAAGCAAATGTTTTGCCGACTACGTTTCTATATTTTCAGCGGATAAAATCAATGACTGGAAACCAATTAAAGAGGGGCAGTGCTTATCTGATTCAATGAAAGGTGATATAAACGCCACAGATTATTTAAAAGTTGTTTTCGTTAGTGATCGTACCGTAAACAAAAAAGGATTTTTAGGTAAAGTGGCTTCAGTATGCGGTGGACTAATAACTGACCTTTCTGGAACCTTTGGACCAGTTTTAGCTGATATTATAAACATTGAATATCCAAATTATAGGTGTGATTGGACTGTAAAAGTACGACCGGGTAGAGTCATAAAAGTTTTATTTGAACATTTTAATATAACAAGTAATGACTGTTCAACTTCGGTGATTTTACATAACGGCGATTCAATTTATGCTCCTATGTTAGGAAGTGGAAAATACTGTGGGCTTGAACACGAAATCAAGGAAAATTTAGTTACTTCAAGTAATACGTTATATGTCAGTTACGTGACCAAGAACTCTTGGAGCAGACTTTCATCCAAATTTGAAAATTTTATTATTCATTACGAAGAACATAGTATAGAGTGCGGATTTACTTCGAAATTGGATCAAGATCAAGCATGGGAAATCATAAATTCCCCGAACTACCCAGCAGTTCCTCAACCATATACAGAGTGTGGTTGGACTATAACTGGGCCTGCTGGTGAAATTTTGAGAGTTGATTTTATAGAAAGGTTTGATTTGGACAACGTAAATAACTGCGAAACGGAATCGGTAGAAATATATGATGGTAGTTCAGCATTGGCTCCTTCCCTAGGCAGATTTTGTCAAGATAAACCTGCAACTGTGAAAACAAAAAGCAATACAGTGTTTGTTCAATATTTTACACAGCTTGCAGAACCAAGGAATGGATTCAAAGCCAACATATCTATTGATGTTTGTGGTGGCACGATAATAGCATCGTCAGGAGAGATTTTATCTCCAGGATATCCTCACTTGCAAATTTTACCTTACGGCACTGAATGCAAGTGGGAAATAATAGGAACGCCTACGAGAATTTTACATTTAAATCCTCAAGACATACAACTACCAGAATCCGAAGCTCCGTGTGCTACTTACATAACAGTCGAGGAAACAATCGTTGCTAATAACACAATTGTTATATTACAAAAATTCTGCAATGATGCTGTTCAACACAATTTGTCTCCAATAGAATCTACCTCAAACAAAATAGTCATTAGACTACATATCGGGAAACCTAGTCAATGGATACAAATTTCAGAGCATAGAGGTTTCAAATTTACTTTTAATACTTCACAACCAACGTGTGGTGGCACAATTACGATACCTGAAGGCTTTTTAACGACACCTAGGTACCCCATGGAAACTTCTTTAAAATATTGTCAGTGGAAAATCGAAGTTCAAAAAAATCGTCGAATACGACTAGAAATCATAGATGCTGACACGCAGAAATTAATAATAAGCATGTATAACGATAACAAATTTCAGTCTTTAATAAGCATACTCTCAGGAGAAGAAAATAACACTGCAAGCCAAATTTTCGAATCATCCGGCAATCAATTATCTTTTTATATATGGTTAAAATCTACGAAAACTCAGTATCGGTTTAAAGCTAAGTTTAGTTCTGATGAACCTTCTTTATGTGGTGATGAACTTCAAGGATTAAAAGGCAGCATAACCTCTCCCGATATAAACAGATCTTATGCTTGTGAATGGCATTACAACTCCGCAGGAGTAATTCTAAATGAAACTTATAAATATTCGACGACCCTTATAAAAATCAACATGACTTCGTCTGTGTCTAGAACACATTGTAGATATTTCGATCCTAAGCTAATGATTGCATCCAAGTCTGTGAGCTTTAGTAAATCAATTTGTGGTAATACCATAACATCCTTAAAAATACCTCTACCTTCTTTCGATTTGAAAGCATTCAAAGGAAACATGAAATCATTAGATTTTACGGTATCCTGGGAATTACAACCATGCGGCGGTATAGTTCATGTGACTGAAAATCCAACTAATATTATTGATGTACCTGGGTCTTATGGTAGTACGATAGATTGTGCATGGCAACTGTCAATTAATGCTAACAACAGAATCCAGATAAATCTAGAAGGTACGTTTAACTTGGAGTGTGATGATGAATATATAAAAGTTTCTCGAGATCTTTCCCAAAACTCTCAAGTGATTGGTGATTTTTGTAAAAGTAATGCATTGACGATACCAATTTTATCGAATTTGAATAATGTTTATGTACAGTACCATTCAAAAGTAAAAAGTAATACAAATATACGATTAATTGCTAAAACCGTTACTAATCAATGCGGTGGTGTTTTGTTTGATTACGAAAAAGTTTTTGCGTCCCCGAACTATCCGAAAAATCATGACGCTAATCTAGAATGTGTATGGGAGATCAAAGCTAACGTAGGAAATCGGGTTAATTTAAAGTTTATTGACCGATTTACAATTGAAGAAACACCAAACTGCACCAAAGACGCTGTTATTATTTATGATTGGAAAGATAATGAGTACCAGGAGATAGCAAAACTTTGTGGTCGTAATGTCCCTCTGTCATATAATTCGACCAACTACAAAATGAAGGTTGTTTTTCGAACAGATTCAGATATTAATCTCGATGGATTCAAAGCGCGTTGGGATCCAATATGTGGCGGCAATTTTATAGCCACAGAAAAAGAACAGTTTTTGTACAGTCCTAACTATCCAGATGAATATCCAAATCTTTTAAACTGCACATATGAAATTTCAGCGCCAGATAAAAAAACGGAAATAAAGTTTGTCGAATTTGAATTGGAAGGTAGCTACCCTGATTGCTCTTATGACAACTTAACTGTATCTTATGCTGAAACTTACGACTATTTCTCAGAAGTATACTGTGGAAAACAGAAACCTCCGATGATGATCGGCGACAAAATTAATCTAGAACTGAAATCCGATGAGTTTTTAACACAAAAAGGTTTCAAAATCGCCTTCAAAACCTTCGATTGTGGCGGCCATATAAACTCCACTACTATGATCAAATCTACCAGAACTGAAAAATATCACGAAAATATGAATTGTACTTGGATTATTAATGCCCCAAAAGATGAAATTGTGATAATTAAATTTATATACATCGATTTAGAGGACCACTATACTTGTCAAAACGACTACATTTCTGTGTATAATGGTCTTACAGATGATGAAGATAAACGCATAGCTTTGTTTTGCGGACTCATAAACAAAACTACAACCGTGAAAAGTACAGGAAATACAATGCTTGTACAGTTCATTTCCGACAGTAGTATGGAGTTGACAGGATTCAAAGCTGAAGTTTATTTTGGTTTATCAGAAACTGTTGGATGTGGTGGAAAGATAGATTTGAGTGATGGTAAGGCTCGAACTGTCAAATCTCCCTTATTAAAAAACAGGGTAGTATATGAAAACTACTTGGATTGTGATTGGGCCATACAATCATTAGATGGTACTTATATAAAAATAGAATTTTTGTCATTTCACATTTCTCCGTGCGGCGACGTCAATCAAACTGCATTGGGCTACAGTAAGTGCGACTGTGATTATGTCGAAATTAAAGATGGAATTTATCCAAACAGTCTAATAATAGGAACATATTGTGGACATGTTATTCCAAGTCCGGTAATATCATCAGGAAACCAAATGAGCATCAAACTCATCACCGACGGAGAAATAGCCAGCTCGGGCTTTGAAGCCAAACTGACTGTGCTACCAACTATTTGTGGTCAATCACATTACGTTGTTAAAGAAACTAGGACGGAGATAAAATCTCCTGGTTATGATATAGGTTCCATTCCACGTGGAACACATTGTATGTACATCCTAGATGCCGGCGATAACCCTTATACAACAGTACGTTTGTCTATCACTACCGACTTACAACCTGTTAATGTTCAATCAAAACGCTGTACCGGAGACAAATTATTGATTACGTACTATAATAGCAACAGTAACGCTACACTTGGAAAAGATTTCATACTACACACTGAAACGACCGATTTCTTTTCACGTTCATCTTTGTATGACCTTACCGTTCCTACAAAGTTTGAATTGTGCGGTCATCAGAAAACATATGACATCTACGTCACCGGAAGCGTATCAATAAATTTAATAACATCTCCGGTGTCCGATTCATTAATTCATAGAGGGGTAAAAATAGATTTCTCATATGCAAGCTACTGCAGCCGAAACTACACCGGGATACAGGGCAGGATAAAAACAGATCACGATGCCCAATATGAGAACATTCATGATTGCTATACACTCATAACCGCACCGGAAAATCATACAATATCACTATACTTTATTAATGTTATACCAAATTATTGGGACGAAAACAGTTTTCTTAGTATATACGACGGCAATAACACGAGCTCACCAAAAATATTAACTATAAATACAATTTACACTGACGCTTCCGTGTTTTCATCGGGCAATTATGTTTTATTACACAATCATCAATCTGATGAGACGCATGCAATTTACGACAGAATCACTTTCGATCTAAATTACGTGGCAACAGATAAAGGTAGGGGTTGTGGCGGTAAGCTGAGTAATGAAATCGGCAAAATAACAAGTCCCCTTTATCCGGAAATCTATAGGCGCCGATCCACATGTGAATGGGAACTCGAGACACCTCCGGGTACACAGCTGGTACTAAGATTTGAAACATTCGATATGGGGATTAACTGTGATGAAAATTATATCCAATTGGTTGATAGTAAAGGTACTATATTATCGTCGTATTGTTCTGAAACACCAGCCGATTTCACTAGTCAAGACAATTATGTTAAAGTCGTAATGTATTCGACTGTTAATAATGGCGGCACCGGTTGGGTCGCTCTCTTCGCTGGCATCGAGGCCGTCTAA
Protein
MNRKLINLQRELALLRVDQCRLQPCMHGGICLSILDGYHCLCPSNWEGQNCDIDVNECHNFAGTDLGCQNGATCINRPGSYECLCKSGWYGLHCTRKAKDCSGGDFEMCGHGTCVPVTTGQGVKCICDQGWTTNGTDFSCLTDVNECEASQGPRCSVNPKVECINLPGSFRCGQCPPGYQGDGYSCSDIDECSTIPNGGCSPVAACHNTIGSRICGPCPLGFQGDGVSCSWKGSCNLDHGGCHPSAQCIDNGRMGGAGAQCICPEGMEGDGYGLNGCFISNGGNQSCASRPCGLNGRCHTLRTGYTCVCRKGFSGAHCEVPSNLCANNPCLNGGVCRLDDQNPRGFRCECTAQYSGPICQLVSKRCGGVLDNNEGTISYPVANTTYNNNARCAWVIHTNPDKVINVTFTKFYLESHPDCLYDFLQIHDGRSSASQLLGRFCGNEFPKGGNIISSHNNLYLWFSSDATVAKNGFTLHWISVKPICGGDVDVTKHGQISSPGSPGKYPPNRDCYWHLSTTLERPIAHKCTLGDYLELRNGVTENSPIIDQLCGNFEKRIILSMANALYIRFHSDFYLSGKGFKLEWDGTVIGCGGTVTSSKGSIASPNYPNNYHDFQECFYKIVASPGSRIHISFVELDLERTHECEDDYIEIYDGLDSSANKLGRFCTMSPELVNIATSSNSAYLKFRSDFYLSGKGFLLNYEAACHNNITGNYGVIETPNFPGFYPANSNCLWNITVSKGNRINVTFTDFNLYKPYRGYPFSRLNTFYRYQTCQHDYIQIKDSADSTFSDKICGNKIPSMITTKENSLQIKFFSGYVPRTGFRLEWVRFGCGGVVRASNGILELEKRFMSSKELECEWTIRTSIGKSLILNFSDIYLSETKDCTEDAIEVYNGEDTTSPLLTKICSRKPTSVQSTANVMFVRLSKLSSLKDVYFKSKYRSIASTCGGSIKSTSGFIYSKNYPKNYDNNLDCLWKIEVAKDHRIALNFTDVDLYSENVAPGHDCNDRIEVYDNMFNMLTKTYKYHICSRSDTKSFVSDSNTIYVKFVTDNVGTAKGFKGNFNTVCGSSITAITDGTISSDKHPYSNSCSWTIKASDLDKKISLSLTHIALPTDFSNFINRTCSSTYLRLYDGDDTNAPEIGEYCGRKIPPLIVSHGSAITMELGTYSNKIEGEFSAHYSTLSNACGGTYTSEEGALASPNYPRPYPSGVDCEWIIKASPGNQIYITFESFNLEFSEACNEDYLELRENSGSGQLLDVYCGNDIPSNVTIGNKLYIKFHSKMQSTVKTNGFLIHYGLLHNNEITGDHGRITSPLYPNLYHDSGDFTWRIITTARKTISIKFDTLNIPTYGDICFNKLSIYDGYDSSGRLLTELCGVTLESDTFETSSNAIFIKFSLDGSNTGSLFSLTWTSSDKIMINEDENEIINCGSNETQTLLPGEIKIIKSPNYPNPYDIDLNCKWEFKGTLGNHLKISFIDFNLEETSKCFADYVSIFSADKINDWKPIKEGQCLSDSMKGDINATDYLKVVFVSDRTVNKKGFLGKVASVCGGLITDLSGTFGPVLADIINIEYPNYRCDWTVKVRPGRVIKVLFEHFNITSNDCSTSVILHNGDSIYAPMLGSGKYCGLEHEIKENLVTSSNTLYVSYVTKNSWSRLSSKFENFIIHYEEHSIECGFTSKLDQDQAWEIINSPNYPAVPQPYTECGWTITGPAGEILRVDFIERFDLDNVNNCETESVEIYDGSSALAPSLGRFCQDKPATVKTKSNTVFVQYFTQLAEPRNGFKANISIDVCGGTIIASSGEILSPGYPHLQILPYGTECKWEIIGTPTRILHLNPQDIQLPESEAPCATYITVEETIVANNTIVILQKFCNDAVQHNLSPIESTSNKIVIRLHIGKPSQWIQISEHRGFKFTFNTSQPTCGGTITIPEGFLTTPRYPMETSLKYCQWKIEVQKNRRIRLEIIDADTQKLIISMYNDNKFQSLISILSGEENNTASQIFESSGNQLSFYIWLKSTKTQYRFKAKFSSDEPSLCGDELQGLKGSITSPDINRSYACEWHYNSAGVILNETYKYSTTLIKINMTSSVSRTHCRYFDPKLMIASKSVSFSKSICGNTITSLKIPLPSFDLKAFKGNMKSLDFTVSWELQPCGGIVHVTENPTNIIDVPGSYGSTIDCAWQLSINANNRIQINLEGTFNLECDDEYIKVSRDLSQNSQVIGDFCKSNALTIPILSNLNNVYVQYHSKVKSNTNIRLIAKTVTNQCGGVLFDYEKVFASPNYPKNHDANLECVWEIKANVGNRVNLKFIDRFTIEETPNCTKDAVIIYDWKDNEYQEIAKLCGRNVPLSYNSTNYKMKVVFRTDSDINLDGFKARWDPICGGNFIATEKEQFLYSPNYPDEYPNLLNCTYEISAPDKKTEIKFVEFELEGSYPDCSYDNLTVSYAETYDYFSEVYCGKQKPPMMIGDKINLELKSDEFLTQKGFKIAFKTFDCGGHINSTTMIKSTRTEKYHENMNCTWIINAPKDEIVIIKFIYIDLEDHYTCQNDYISVYNGLTDDEDKRIALFCGLINKTTTVKSTGNTMLVQFISDSSMELTGFKAEVYFGLSETVGCGGKIDLSDGKARTVKSPLLKNRVVYENYLDCDWAIQSLDGTYIKIEFLSFHISPCGDVNQTALGYSKCDCDYVEIKDGIYPNSLIIGTYCGHVIPSPVISSGNQMSIKLITDGEIASSGFEAKLTVLPTICGQSHYVVKETRTEIKSPGYDIGSIPRGTHCMYILDAGDNPYTTVRLSITTDLQPVNVQSKRCTGDKLLITYYNSNSNATLGKDFILHTETTDFFSRSSLYDLTVPTKFELCGHQKTYDIYVTGSVSINLITSPVSDSLIHRGVKIDFSYASYCSRNYTGIQGRIKTDHDAQYENIHDCYTLITAPENHTISLYFINVIPNYWDENSFLSIYDGNNTSSPKILTINTIYTDASVFSSGNYVLLHNHQSDETHAIYDRITFDLNYVATDKGRGCGGKLSNEIGKITSPLYPEIYRRRSTCEWELETPPGTQLVLRFETFDMGINCDENYIQLVDSKGTILSSYCSETPADFTSQDNYVKVVMYSTVNNGGTGWVALFAGIEAV

Summary

Description
Required in the nephrocyte for normal uptake of proteins and elimination of toxins, and for maintenance of endocytic trafficking structures. May function together with Amnionless.
Cotransporter which plays a role in lipoprotein, vitamin and iron metabolism, by facilitating their uptake. Binds to ALB, MB, Kappa and lambda-light chains, TF, hemoglobin, GC, SCGB1A1, APOA1, high density lipoprotein, and the CBLIF-cobalamin complex. The binding of all ligands requires calcium. Serves as important transporter in several absorptive epithelia, including intestine, renal proximal tubules and embryonic yolk sac. Interaction with LRP2 mediates its trafficking throughout vesicles and facilitates the uptake of specific ligands like GC, hemoglobin, ALB, TF and SCGB1A1. Interaction with AMN controls its trafficking to the plasma membrane and facilitates endocytosis of ligands. May play an important role in the development of the peri-implantation embryo through internalization of APOA1 and cholesterol. Binds to LGALS3 at the maternal-fetal interface (By similarity).
Cotransporter which plays a role in lipoprotein, vitamin and iron metabolism, by facilitating their uptake. Binds to ALB, MB, Kappa and lambda-light chains, TF, hemoglobin, GC, SCGB1A1, APOA1, high density lipoprotein, and the CBLIF-cobalamin complex. The binding of all ligands requires calcium. Serves as important transporter in several absorptive epithelia, including intestine, renal proximal tubules and embryonic yolk sac. Interaction with LRP2 mediates its trafficking throughout vesicles and facilitates the uptake of specific ligands like GC, hemoglobin, ALB, TF and SCGB1A1. Interaction with AMN controls its trafficking to the plasma membrane and facilitates endocytosis of ligands. May play an important role in the development of the peri-implantation embryo through internalization of APOA1 and cholesterol. Binds to LGALS3 at the maternal-fetal interface.
Cotransporter which plays a role in lipoprotein, vitamin and iron metabolism, by facilitating their uptake.
Protease which specifically processes prolysyl oxidase and maybe also chordin. Required for the embryonic development. Predominant protease, which in the development, influences dorsal-ventral patterning and skeletogenesis. In embryos, inhibits the development of dorsoanterior structures and ventralizes activin-induced dorsal mesoderm in animal caps.
Protease which processes procollagen C-propeptides, such as chordin. Required for the embryonic development. Predominant protease, which in the development, influences dorsal-ventral patterning and skeletogenesis.
Protease which processes procollagen C-propeptides, such as chordin, probiglycan and prolysyl oxidase. Required for the embryonic development. Predominant protease, which in the development, influences dorsal-ventral patterning and skeletogenesis (By similarity).
Required for patterning ventral tissues of the tail. May increase bone morphogenetic protein (BMP) activity at the end of gastrulation by proteolytic cleavage of chordin and release of BMP from inactive complexes.
Protease which processes procollagen C-propeptides, such as chordin, pro-biglycan and pro-lysyl oxidase. Required for the embryonic development, especially heart development. Predominant protease, which in the development, influences dorsal-ventral patterning and skeletogenesis.
Cleaves the C-terminal propeptides of procollagen I, II and III. Induces cartilage and bone formation. May participate in dorsoventral patterning during early development by cleaving chordin (CHRD) (By similarity). Responsible for the proteolytic activation of lysyl oxidase LOX.
May play roles in mucosal defense system and cellular immune defense. May play a role in liver regeneration. May be an important factor in fate decision and differentiation of transit-amplifying ductular (oval) cells within the hepatic lineage. May function as a binding protein in saliva for the regulation of taste sensation. May play a role as an opsonin receptor for SFTPD and SPAR in macrophage tissues throughout the body, including epithelial cells lining the gastrointestinal tract (By similarity). Required for terminal differentiation of columnar epithelial cells during early embryogenesis. Displays a broad calcium-dependent binding spectrum against both Gram-positive and Gram-negative bacteria, suggesting a role in defense against bacterial pathogens. Binds to a range of poly-sulfated and poly-phosphorylated ligands which may explain its broad bacterial-binding specificity. Inhibits cytoinvasion of S.enterica. Associates with the actin cytoskeleton and is involved in its remodeling during regulated exocytosis. Interacts with pancreatic zymogens in a pH-dependent manner and may act as a Golgi cargo receptor in the regulated secretory pathway of the pancreatic acinar cell.
Functions as a receptor for membrane-bound ligands Jagged-1 (JAG1), Jagged-2 (JAG2) and Delta-1 (DLL1) to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs. Involved in angiogenesis; negatively regulates endothelial cell proliferation and migration and angiogenic sprouting. Involved in the maturation of both CD4(+) and CD8(+) cells in the thymus. Important for follicular differentiation and possibly cell fate selection within the follicle. During cerebellar development, functions as a receptor for neuronal DNER and is involved in the differentiation of Bergmann glia. Represses neuronal and myogenic differentiation. May play an essential role in postimplantation development, probably in some aspect of cell specification and/or differentiation. May be involved in mesoderm development, somite formation and neurogenesis. May enhance HIF1A function by sequestering HIF1AN away from HIF1A. Required for the THBS4 function in regulating protective astrogenesis from the subventricular zone (SVZ) niche after injury. Involved in determination of left/right symmetry by modulating the balance between motile and immotile (sensory) cilia at the left-right organiser (LRO).
Functions as a receptor for membrane-bound ligands Jagged-1 (JAG1), Jagged-2 (JAG2) and Delta-1 (DLL1) to regulate cell-fate determination (By similarity). Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus (By similarity). Affects the implementation of differentiation, proliferation and apoptotic programs (By similarity). Involved in angiogenesis; negatively regulates endothelial cell proliferation and migration and angiogenic sprouting (By similarity). Involved in the maturation of both CD4(+) and CD8(+) cells in the thymus (By similarity). Important for follicular differentiation and possibly cell fate selection within the follicle (By similarity). During cerebellar development, functions as a receptor for neuronal DNER and is involved in the differentiation of Bergmann glia (PubMed:11182080). Represses neuronal and myogenic differentiation (By similarity). May play an essential role in postimplantation development, probably in some aspect of cell specification and/or differentiation (By similarity). May be involved in mesoderm development, somite formation and neurogenesis (By similarity). May enhance HIF1A function by sequestering HIF1AN away from HIF1A (By similarity). Required for the THBS4 function in regulating protective astrogenesis from the subventricular zone (SVZ) niche after injury (By similarity). Involved in determination of left/right symmetry by modulating the balance between motile and immotile (sensory) cilia at the left-right organiser (LRO) (By similarity).
Functions as a receptor for membrane-bound ligands Jagged-1 (JAG1), Jagged-2 (JAG2) and Delta-1 (DLL1) to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs. Involved in angiogenesis; negatively regulates endothelial cell proliferation and migration and angiogenic sprouting. Involved in the maturation of both CD4(+) and CD8(+) cells in the thymus. Important for follicular differentiation and possibly cell fate selection within the follicle. During cerebellar development, functions as a receptor for neuronal DNER and is involved in the differentiation of Bergmann glia. Represses neuronal and myogenic differentiation. May play an essential role in postimplantation development, probably in some aspect of cell specification and/or differentiation. May be involved in mesoderm development, somite formation and neurogenesis. May enhance HIF1A function by sequestering HIF1AN away from HIF1A (By similarity). Required for the THBS4 function in regulating protective astrogenesis from the subventricular zone (SVZ) niche after injury. Involved in determination of left/right symmetry by modulating the balance between motile and immotile (sensory) cilia at the left-right organiser (LRO) (By similarity).
Functions as a receptor for membrane-bound ligands Jagged-1 (JAG1), Jagged-2 (JAG2) and Delta-1 (DLL1) to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs. Involved in angiogenesis; negatively regulates endothelial cell proliferation and migration and angiogenic sprouting. Involved in the maturation of both CD4(+) and CD8(+) cells in the thymus. Important for follicular differentiation and possibly cell fate selection within the follicle. During cerebellar development, functions as a receptor for neuronal DNER and is involved in the differentiation of Bergmann glia. Represses neuronal and myogenic differentiation. May play an essential role in postimplantation development, probably in some aspect of cell specification and/or differentiation. May be involved in mesoderm development, somite formation and neurogenesis (By similarity). Involved in determination of left/right symmetry by modulating the balance between motile and immotile (sensory) cilia at the left-right organiser (LRO).
Functions as a receptor for membrane-bound ligands Jagged1, Jagged2 and Delta1 to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs. May regulate branching morphogenesis in the developing vascular system (By similarity).
Functions as a receptor for membrane-bound ligands Jagged1, Jagged2 and Delta1 to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs (By similarity). May regulate branching morphogenesis in the developing vascular system.
Functions as a receptor for membrane-bound ligands Jagged-1 (JAG1), Jagged-2 (JAG2) and Delta-1 (DLL1) to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs. Involved in angiogenesis; negatively regulates endothelial cell proliferation and migration and angiogenic sprouting. Involved in the maturation of both CD4(+) and CD8(+) cells in the thymus. Important for follicular differentiation and possibly cell fate selection within the follicle. During cerebellar development, functions as a receptor for neuronal DNER and is involved in the differentiation of Bergmann glia. Represses neuronal and myogenic differentiation. May play an essential role in postimplantation development, probably in some aspect of cell specification and/or differentiation. May be involved in mesoderm development, somite formation and neurogenesis. Involved in determination of left/right symmetry by modulating the balance between motile and immotile (sensory) cilia at the left-right organiser (LRO) (By similarity).
Functions as a receptor for membrane-bound ligands Jagged-1 (JAG1), Jagged-2 (JAG2) and Delta-1 (DLL1) to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus (PubMed:21378985, PubMed:21378989). Affects the implementation of differentiation, proliferation and apoptotic programs (By similarity). Involved in bone remodeling and homeostasis. In collaboration with RELA/p65 enhances NFATc1 promoter activity and positively regulates RANKL-induced osteoclast differentiation (PubMed:29149593). Positively regulates self-renewal of liver cancer cells (PubMed:25985737).
Involved in several cell fate decisions that require cell-cell interactions. It is possible that lin-12 encodes a membrane-bound receptor for a signal that enables expression of the ventral uterine precursor cell fate. Activity in cell fate decisions and tumorigenesis is negatively regulated by sel-10.
Functions as a receptor for membrane-bound ligands Jagged-1 (JAG1), Jagged-2 (JAG2) and Delta-1 (DLL1) to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs. Involved in angiogenesis; negatively regulates endothelial cell proliferation and migration and angiogenic sprouting. Involved in the maturation of both CD4(+) and CD8(+) cells in the thymus. Important for follicular differentiation and possibly cell fate selection within the follicle. During cerebellar development, functions as a receptor for neuronal DNER and is involved in the differentiation of Bergmann glia. Represses neuronal and myogenic differentiation. May play an essential role in postimplantation development, probably in some aspect of cell specification and/or differentiation. May be involved in mesoderm development, somite formation and neurogenesis (By similarity). Involved in determination of left/right symmetry by modulating the balance between motile and immotile (sensory) cilia at the left-right organiser (LRO) (By similarity).
Functions as a receptor for membrane-bound ligands Jagged1, Jagged2 and Delta1 to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs (By similarity). May play a role during CNS development.
Functions as a receptor for membrane-bound ligands Jagged-1 (JAG1), Jagged-2 (JAG2) and Delta-1 (DLL1) to regulate cell-fate determination (PubMed:10393120). Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus (PubMed:10393120, PubMed:18710934). Affects the implementation of differentiation, proliferation and apoptotic programs (PubMed:10393120, PubMed:18710934). May play an essential role in postimplantation development, probably in some aspect of cell specification and/or differentiation (By similarity). In collaboration with RELA/p65 enhances NFATc1 promoter activity and positively regulates RANKL-induced osteoclast differentiation (PubMed:18710934). Positively regulates self-renewal of liver cancer cells (By similarity).
Functions as a receptor for membrane-bound ligands Jagged-1 (JAG1), Jagged-2 (JAG2) and Delta-1 (DLL1) to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs (By similarity). Involved in bone remodeling and homeostasis. In collaboration with RELA/p65 enhances NFATc1 promoter activity and positively regulates RANKL-induced osteoclast differentiation. Positively regulates self-renewal of liver cancer cells (By similarity).
Required to maintain the integrity of photoreceptor cells (PubMed:27737822, PubMed:28378834, PubMed:30052645). Specifically required for normal morphology of the photoreceptor ciliary pocket, and might thus facilitate protein trafficking between the photoreceptor inner and outer segments via the transition zone (PubMed:27737822).
Functions as a receptor for membrane-bound ligands Jagged1, Jagged2 and Delta1 to regulate cell-fate determination. Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs (By similarity). Acts instructively to control the cell fate determination of CNS multipotent progenitor cells, resulting in astroglial induction and neuron/oligodendrocyte suppression.
Required to maintain the integrity of photoreceptor cells (PubMed:18836446). Specifically required for normal morphology of the photoreceptor ciliary pocket, and might thus facilitate protein trafficking between the photoreceptor inner and outer segments via the transition zone (By similarity).
Ligand for Notch receptors and involved in the mediation of Notch signaling (By similarity). Seems to be involved in cell-fate decisions.
Required to maintain the integrity of photoreceptor cells (By similarity). Specifically required for normal morphology of the photoreceptor ciliary pocket, and might thus facilitate protein trafficking between the photoreceptor inner and outer segments via the transition zone (By similarity).
Ligand for multiple Notch receptors and involved in the mediation of Notch signaling (By similarity). Seems to be involved in cell-fate decisions.
Functions as a receptor for membrane-bound ligands Jagged1, Jagged2 and Delta1 to regulate cell-fate determination (PubMed:15350543). Upon ligand activation through the released notch intracellular domain (NICD) it forms a transcriptional activator complex with RBPJ/RBPSUH and activates genes of the enhancer of split locus. Affects the implementation of differentiation, proliferation and apoptotic programs (By similarity).
Apical polarity protein that plays a central role during the epithelial-to-mesenchymal transition (EMT) at gastrulation, when newly specified mesodermal cells move inside the embryo. Acts by promoting cell ingression, the process by which cells leave the epithelial epiblast and move inside the embryo to form a new tissue layer. The anisotropic distribution of CRB2 and MYH10/myosin-IIB at cell edges define which cells will ingress: cells with high apical CRB2 are probably extruded from the epiblast by neighboring cells with high levels of apical MYH10/myosin-IIB. Also required for maintenance of the apical polarity complex during development of the cortex.
Ligand for multiple Notch receptors and involved in the mediation of Notch signaling (PubMed:18660822, PubMed:20437614). May be involved in cell-fate decisions during hematopoiesis (PubMed:9462510). Seems to be involved in early and late stages of mammalian cardiovascular development. Inhibits myoblast differentiation (By similarity). Enhances fibroblast growth factor-induced angiogenesis (in vitro).
Essential signaling protein which has a major role in many developmental processes (PubMed:3935325). Functions as a receptor for membrane-bound ligands Delta and Serrate to regulate cell-fate determination (PubMed:10935637, PubMed:15620650, PubMed:12909620, PubMed:18243100). Upon ligand activation, and releasing from the cell membrane, the Notch intracellular domain (NICD) forms a transcriptional activator complex with Su(H) (Suppressor of hairless) and activates genes of the E(spl) complex (PubMed:7671825). Regulates oogenesis, the differentiation of the ectoderm and the development of the central and peripheral nervous system, eye, wing disk, muscles and segmental appendages such as antennae and legs, through lateral inhibition or induction (PubMed:11719214, PubMed:12369105, PubMed:3935325). Regulates neuroblast self-renewal, identity and proliferation through the regulation of bHLH-O proteins; in larval brains, involved in the maintenance of type II neuroblast self-renewal and identity by suppressing erm expression together with pnt; might also regulate dpn expression through the activation of the transcriptional regulator Su(H) (PubMed:27151950, PubMed:28899667, PubMed:20152183, PubMed:18342578, PubMed:23056424, PubMed:21262215).
Ligand for multiple Notch receptors and involved in the mediation of Notch signaling. May be involved in cell-fate decisions during hematopoiesis. Seems to be involved in early and late stages of mammalian cardiovascular development. Inhibits myoblast differentiation (By similarity). May regulate fibroblast growth factor-induced angiogenesis.
Apical polarity protein that plays a central role during the epithelial-to-mesenchymal transition (EMT) at gastrulation, when newly specified mesodermal cells move inside the embryo (PubMed:26496195, PubMed:27870829). Acts by promoting cell ingression, the process by which cells leave the epithelial epiblast and move inside the embryo to form a new tissue layer (PubMed:27870829). The anisotropic distribution of CRB2 and MYH10/myosin-IIB at cell edges define which cells will ingress: cells with high apical CRB2 are probably extruded from the epiblast by neighboring cells with high levels of apical MYH10/myosin-IIB (PubMed:27870829). Also required for maintenance of the apical polarity complex during development of the cortex.
Putative Notch ligand involved in the mediation of Notch signaling. Involved in limb development (By similarity).
Involved in the specification of the cell fates of the blastomeres, ABa and APa (PubMed:8156602). Proper signaling by glp-1 induces ABa descendants to produce anterior pharyngeal cells, and APa descendants to adopt a different fate (PubMed:8156602). Contributes to the establishment of the dorsal-ventral axis in early embryos (PubMed:8156602). Regulates germ cell mitotic proliferation probably by regulating MAP kinase phosphatase lip-1 expression (PubMed:22278922, PubMed:16319922). Plays a negative role in lifespan (PubMed:24332851, PubMed:28853436).
Plays a central role in cell polarity establishment (PubMed:2344615, PubMed:12900452, PubMed:10102271, PubMed:11740560). Participates in the assembly, positioning and maintenance of adherens junctions via its interaction with the SAC complex (PubMed:11740560, PubMed:12900452, PubMed:10102271, PubMed:11076972). Controls the coalescence of the spots of zonula adherens (ZA) into a adhesive ring around the cells (PubMed:11740560). It may act as a signal (PubMed:2344615). Involved in morphogenesis of the photoreceptor rhabdomere, for positioning and growth of rhabdomere and AJ during the crucial period of photoreceptor extension along the proximodistal axis of the retina (PubMed:12900452). Component of the crb-galla-Xpd (CGX) complex which is essential for proper mitotic chromosome segregation in early embryos (PubMed:25065591). The CGX complex is also required for cell proliferation in developing wing disks (PubMed:25065591). In the CGX complex, acts with galla-1 or galla-2 to recruit Xpd and thus form the functional complex. Together with apn, plays a key role in trachea development at larval stages (PubMed:30645584).
Transmembrane ligand protein of NOTCH1, NOTCH2 and NOTCH3 receptors that binds the extracellular domain (ECD) of Notch receptor in a cis and trans fashion manner (PubMed:21985982, PubMed:10958687). Following transinteraction, ligand cells produce mechanical force that depends of a clathrin-mediated endocytosis, requiring ligand ubiquitination, EPN1 interaction, and actin polymerisation; these events promote Notch receptor extracellular domain (NECD) transendocytosis and triggers Notch signaling through induction of cleavage, hyperphosphorylation, and nuclear accumulation of the intracellular domain of Notch receptors (NICD) (PubMed:10958687, PubMed:18676613). Is required for embryonic development and maintenance of adult stem cells in many different tissues and immune systeme; the DLL1-induced Notch signaling is mediated through an intercellular communication that regulates cell lineage, cell specification, cell patterning and morphogenesis through effects on differentiation and proliferation (PubMed:17194759, PubMed:19562077, PubMed:18997111, PubMed:23695674, PubMed:16495313, PubMed:21238454, PubMed:22282195, PubMed:7671806, PubMed:17960184, PubMed:22529374, PubMed:19389377, PubMed:23699523, PubMed:19144989, PubMed:23688253, PubMed:23806616, PubMed:26114479, PubMed:22940113, PubMed:25220152, PubMed:20081190, PubMed:21572390, PubMed:22096075). Plays a role in brain development at different level, namely by regulating neuronal differentiation of neural precursor cells via cell-cell interaction, most likely through the lateral inhibitory system in an endogenous level dependent-manner (PubMed:7671806, PubMed:18997111). During neocortex development, Dll1-Notch signaling transmission is mediated by dynamic interactions between intermediate neurogenic progenitors and radial glia; the cell-cell interactions are mediated via dynamic and transient elongation processes, likely to reactivate/maintain Notch activity in neighboring progenitors, and coordinate progenitor cell division and differentiation across radial and zonal boundaries (PubMed:23699523). During cerebellar development, regulates Bergmann glial monolayer formation and its morphological maturation through a Notch signaling pathway (PubMed:23688253). At the retina and spinal cord level, regulates neurogenesis by preventing the premature differentiation of neural progenitors and also by maintaining progenitors in spinal cord through Notch signaling pathway (PubMed:19389377, PubMed:26114479). Also controls neurogenesis of the neural tube in a progenitor domain-specific fashion along the dorsoventral axis (PubMed:20081190). Maintains quiescence of neural stem cells and plays a role as a fate determinant that segregates asymmetrically to one daughter cell during neural stem cells mitosis, resulting in neuronal differentiation in Dll1-inheriting cell (PubMed:23695674). Plays a role in immune systeme development, namely the development of all T-cells and marginal zone (MZ) B cells (PubMed:15146182, PubMed:19217325). Blocks the differentiation of progenitor cells into the B-cell lineage while promoting the emergence of a population of cells with the characteristics of a T-cell/NK-cell precursor (By similarity). Upon MMP14 cleavage, negatively regulates Notch signaling in haematopoietic progenitor cells to specifically maintain normal B-cell development in bone marrow (PubMed:21572390). Also plays a role during muscle development. During early development, inhibits myoblasts differentiation from the medial dermomyotomal lip and later regulates progenitor cell differentiation (PubMed:17194759). Directly modulates cell adhesion and basal lamina formation in satellite cells through Notch signaling. Maintains myogenic progenitors pool by suppressing differentiation through down-regulation of MYOD1 and is required for satellite cell homing and PAX7 expression (PubMed:22940113). During craniofacial and trunk myogenesis suppresses differentiation of cranial mesoderm-derived and somite-derived muscle via MYOD1 regulation but in cranial mesoderm-derived progenitors, is neither required for satellite cell homing nor for PAX7 expression (PubMed:25220152). Also plays a role during pancreatic cell development. During type B pancreatic cell development, may be involved in the initiation of proximodistal patterning in the early pancreatic epithelium (PubMed:22529374). Stimulates multipotent pancreatic progenitor cells proliferation and pancreatic growth by maintaining HES1 expression and PTF1A protein levels (PubMed:22096075). During fetal stages of development, is required to maintain arterial identity and the responsiveness of arterial endothelial cells for VEGFA through regulation of KDR activation and NRP1 expression (PubMed:19144989). Controls sprouting angiogenesis and subsequent vertical branch formation througth regulation on tip cell differentiation (PubMed:22282195). Negatively regulates goblet cell differentiation in intestine and controls secretory fat commitment through lateral inhibition in small intestine (PubMed:21238454, PubMed:21915337). Plays a role during inner ear development; negatively regulates auditory hair cell differentiation (PubMed:16495313). Plays a role during nephron development through Notch signaling pathway (PubMed:23806616). Regulates growth, blood pressure and energy homeostasis (PubMed:19562077).
Plays a role in photoreceptor morphogenesis in the retina. May maintain cell polarization and adhesion. Isoform 3 could play a role in epidermal tissue morphogenesis. May function in cell attachment for stratified epithelial organization.
Ligand for tyrosine-protein kinase receptors AXL, TYRO3 and MER whose signaling is implicated in cell growth and survival, cell adhesion and cell migration. GAS6/AXL signaling plays a role in various processes such as endothelial cell survival during acidification by preventing apoptosis, optimal cytokine signaling during human natural killer cell development, hepatic regeneration, gonadotropin-releasing hormone neuron survival and migration, platelet activation, or regulation of thrombotic responses.
(Microbial infection) Can bridge virus envelope phosphatidylserine to the TAM receptor tyrosine kinase Axl to mediate viral entry by apoptotic mimicry (PubMed:21501828). Plays a role in Dengue cell entry by apoptotic mimicry (PubMed:23084921). Plays a role in Vaccinia virus cell entry by apoptotic mimicry (PubMed:21501828). Plays a role in ebolavirus and marburgvirus cell entry by apoptotic mimicry (PubMed:17005688).
Transmembrane ligand protein of NOTCH1, NOTCH2 and NOTCH3 receptors that binds the extracellular domain (ECD) of Notch receptor in a cis and trans fashion manner (By similarity). Following transinteraction, ligand cells produce mechanical force that depends of a clathrin-mediated endocytosis, requiring ligand ubiquitination, EPN1 interaction, and actin polymerisation; these events promote Notch receptor extracellular domain (NECD) transendocytosis and triggers Notch signaling through induction of cleavage, hyperphosphorylation, and nuclear accumulation of the intracellular domain of Notch receptors (NICD) (PubMed:22658936). Is required for embryonic development and maintenance of adult stem cells in many different tissues and immune systeme; the DLL1-induced Notch signaling is mediated through an intercellular communication that regulates cell lineage, cell specification, cell patterning and morphogenesis through effects on differentiation and proliferation (By similarity). Plays a role in brain development at different level, namely by regulating neuronal differentiation of neural precursor cells via cell-cell interaction, most likely through the lateral inhibitory system in an endogenous level dependent-manner. During neocortex development, Dll1-Notch signaling transmission is mediated by dynamic interactions between intermediate neurogenic progenitors and radial glia; the cell-cell interactions are mediated via dynamic and transient elongation processes, likely to reactivate/maintain Notch activity in neighboring progenitors, and coordinate progenitor cell division and differentiation across radial and zonal boundaries. During cerebellar development, regulates Bergmann glial monolayer formation and its morphological maturation through a Notch signaling pathway. At the retina and spinal cord level, regulates neurogenesis by preventing the premature differentiation of neural progenitors and also by maintaining progenitors in spinal cord through Notch signaling pathway. Also controls neurogenesis of the neural tube in a progenitor domain-specific fashion along the dorsoventral axis. Maintains quiescence of neural stem cells and plays a role as a fate determinant that segregates asymmetrically to one daughter cell during neural stem cells mitosis, resulting in neuronal differentiation in Dll1-inheriting cell. Plays a role in immune systeme development, namely the development of all T-cells and marginal zone (MZ) B cells (By similarity). Blocks the differentiation of progenitor cells into the B-cell lineage while promoting the emergence of a population of cells with the characteristics of a T-cell/NK-cell precursor (By similarity). Also plays a role during muscle development. During early development, inhibits myoblasts differentiation from the medial dermomyotomal lip and later regulates progenitor cell differentiation. Directly modulates cell adhesion and basal lamina formation in satellite cells through Notch signaling. Maintains myogenic progenitors pool by suppressing differentiation through down-regulation of MYOD1 and is required for satellite cell homing and PAX7 expression. During craniofacial and trunk myogenesis suppresses differentiation of cranial mesoderm-derived and somite-derived muscle via MYOD1 regulation but in cranial mesoderm-derived progenitors, is neither required for satellite cell homing nor for PAX7 expression. Also plays a role during pancreatic cell development. During type B pancreatic cell development, may be involved in the initiation of proximodistal patterning in the early pancreatic epithelium. Stimulates multipotent pancreatic progenitor cells proliferation and pancreatic growth by maintaining HES1 expression and PTF1A protein levels. During fetal stages of development, is required to maintain arterial identity and the responsiveness of arterial endothelial cells for VEGFA through regulation of KDR activation and NRP1 expression. Controls sprouting angiogenesis and subsequent vertical branch formation througth regulation on tip cell differentiation. Negatively regulates goblet cell differentiation in intestine and controls secretory fat commitment through lateral inhibition in small intestine. Plays a role during inner ear development; negatively regulates auditory hair cell differentiation. Plays a role during nephron development through Notch signaling pathway. Regulates growth, blood pressure and energy homeostasis (By similarity).
Acts as a ligand for Notch receptors and is involved in primary neurogenesis. Can activate Notch receptors, thereby playing a key role in lateral inhibition, a process that prevents the immediate neighbors of each nascent neural cell from simultaneously embarking on neural differentiation. Required for boundary formation during segmentation of the hindbrain. Required for midline cell fate specification prior to germ layer formation; regulates specification of floorplate, notochord and hypochord. In inner ear, it prevents adjacent cells from adopting the same cell fate. Plays a role in angiogenesis.
May play a role in the cell attachment process.
Acts as a ligand for Notch receptors and is involved in primary neurogenesis and somitogenesis. Can activate Notch receptors, thereby playing a key role in lateral inhibition, a process that prevents the immediate neighbors of each nascent neural cell from simultaneously embarking on neural differentiation. Required in somite segmentation to keep the oscillations of neighboring presomitic mesoderm cells synchronized.
Acts as a ligand for Notch receptors and is involved in somitogenesis. Can activate Notch receptors. Required in somite segmentation to keep the oscillations of neighboring presomitic mesoderm cells synchronized.
Acts as a ligand for Notch (N) receptor. Essential for proper differentiation of ectoderm. Dl is required for the correct separation of neural and epidermal cell lineages. Fringe (fng) acts in the Golgi to determine the type of O-linked fucose on the EGF modules in N, altering the ability of N to bind with Delta (Dl). O-fut1 also has a role in modulating the interaction.
Acts as a scavenger receptor for acetylated low density lipoprotein. Binds to both Gram-positive and Gram-negative bacteria and may play a role in defense against bacterial infection. When inhibited in endothelial tube formation assays, there is a marked decrease in cell-cell interactions, suggesting a role in angiogenesis. Involved in the delivery of newly synthesized CHID1/SI-CLP from the biosynthetic compartment to the endosomal/lysosomal system.
Phosphatidylserine receptor that enhances the engulfment of apoptotic cells. Hyaluronan receptor that binds to and mediates endocytosis of hyaluronic acid (HA). Acts also, in different species, as a primary systemic scavenger receptor for heparin (Hep), chondroitin sulfate (CS), dermatan sulfate (DS), nonglycosaminoglycan (GAG), acetylated low-density lipoprotein (AcLDL), pro-collagen propeptides and advanced glycation end products (AGE). May serve to maintain tissue integrity by supporting extracellular matrix turnover or it may contribute to maintaining fluidity of bodily liquids by resorption of hyaluronan. Counter receptor which plays an important role in lymphocyte recruitment in the hepatic vasculature. Binds to both Gram-positive and Gram-negative bacteria and may play a role in defense against bacterial infection. The proteolytically processed short form also functions as an endocytosis receptor for heparin internalisation as well as HA and CS.
Adhesive glycoprotein that mediates cell-to-cell and cell-to-matrix interactions and is involved in various processes including cellular proliferation, migration, adhesion and attachment, inflammatory response to CNS injury, regulation of vascular inflammation and adaptive responses of the heart to pressure overload and in myocardial function and remodeling. Binds to structural extracellular matrix (ECM) proteins and modulates the ECM in response to tissue damage, contributing to cardioprotective and adaptive ECM remodeling. Plays a role in ER stress response, via its interaction with the activating transcription factor 6 alpha (ATF6) which produces adaptive ER stress response factors and protects myocardium from pressure overload. May contribute to spinal presynaptic hypersensitivity and neuropathic pain states after peripheral nerve injury. May play a role in regulating protective astrogenesis from the subventricular zone (SVZ) niche after injury in a NOTCH1-dependent manner (By similarity).
Catalytic Activity
Cleavage of the C-terminal propeptide at Ala-|-Asp in type I and II procollagens and at Arg-|-Asp in type III.
Cofactor
Zn(2+)
Subunit
Interacts with LRP2 in a dual-receptor complex in a calcium-dependent manner. Component of the cubam complex composed of CUBN and AMN. The cubam complex can oligomerize and form cubam trimers. Found in a complex with PID1/PCLI1, LRP1 and CUBNI. Interacts with LRP1 and PID1/PCLI1 (By similarity).
Component of the cubam complex composed of CUBN and AMN (By similarity). The cubam complex can oligomerize and form cubam trimers. Interacts with LRP2 in a dual-receptor complex in a calcium-dependent manner. Found in a complex with PID1/PCLI1, LRP1 and CUBNI (By similarity). Interacts with LRP1 and PID1/PCLI1 (By similarity).
Interacts with LRP2 in a dual-receptor complex in a calcium-dependent manner (By similarity). Component of the cubam complex composed of CUBN and AMN. The cubam complex can oligomerize and form cubam trimers. Found in a complex with PID1/PCLI1, LRP1 and CUBNI (By similarity). Interacts with LRP1 and PID1/PCLI1 (By similarity).
Interacts with LRP2 in a dual-receptor complex in a calcium-dependent manner. Component of the cubam complex composed of CUBN and AMN. The cubam complex can oligomerize and form cubam trimers. Found in a complex with PID1/PCLI1, LRP1 and CUBNI. Interacts with LRP1 and PID1/PCLI1.
Interacts with POSTN, the interaction promotes deposition on the extracellular matrix.
Interacts with LGALS3. Binds SPAR in a calcium-dependent manner (By similarity). Binds SFTPD in a calcium-dependent manner.
Heterodimer of a C-terminal fragment N(TM) and an N-terminal fragment N(EC) which are probably linked by disulfide bonds. Interacts with DNER, DTX1, DTX2 and RBPJ/RBPSUH. Also interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH1. Notch 1 intracellular domain interacts with SNW1; the interaction involves multimerized NOTCH1 NICD and is implicated in a formation of an intermediate preactivation complex which associates with DNA-bound CBF-1/RBPJ. The activated membrane-bound form interacts with AAK1 which promotes NOTCH1 stabilization. Forms a trimeric complex with FBXW7 and SGK1. Interacts with HIF1AN. HIF1AN negatively regulates the function of notch intracellular domain (NICD), accelerating myogenic differentiation. Interacts (via NICD) with SNAI1 (via zinc fingers); the interaction induces SNAI1 degradation via MDM2-mediated ubiquitination and inhibits SNAI1-induced cell invasion. Interacts (via NICD) with MDM2A. Interacts (via NICD) with BCL6; the interaction decreases MAML1 recruitment by NOTCH1 NICD on target genes DNA and inhibits NOTCH1 transcractivation activity. Interacts with THBS4. Interacts (via the EGF-like repeat region) with CCN3 (via CTCK domain) (PubMed:12050162). Interacts (via EGF-like domains) with DLL4 (via N-terminal DSL and MNNL domains) (By similarity). Interacts with ZMIZ1. Interacts (via NICD domain) with MEGF10 (via the cytoplasmic domain) (PubMed:28498977). Interacts with DLL1 and JAG1 (PubMed:28089369). Interacts (via NICD domain) with PRAG1 (PubMed:25038227). Forms a complex with PRAG1, N1ICD and MAML1, in a MAML1-dependent manner (PubMed:25038227). Interacts (via transmembrane region) with PSEN1; the interaction is direct (By similarity).
Heterodimer of a C-terminal fragment N(TM) and an N-terminal fragment N(EC) which are probably linked by disulfide bonds. Interacts with DNER, DTX1, DTX2 and RBPJ/RBPSUH. Also interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH1. Notch 1 intracellular domain interacts with SNW1; the interaction involves multimerized NOTCH1 NICD and is implicated in a formation of an intermediate preactivation complex which associates with DNA-bound CBF-1/RBPJ. The activated membrane-bound form interacts with AAK1 which promotes NOTCH1 stabilization. Forms a trimeric complex with FBXW7 and SGK1. Interacts with HIF1AN. HIF1AN negatively regulates the function of notch intracellular domain (NICD), accelerating myogenic differentiation. Interacts (via NICD) with SNAI1 (via zinc fingers); the interaction induces SNAI1 degradation via MDM2-mediated ubiquitination and inhibits SNAI1-induced cell invasion. Interacts (via NICD) with MDM2A. Interacts (via NICD) with BCL6; the interaction decreases MAML1 recruitment by NOTCH1 NICD on target genes DNA and inhibits NOTCH1 transcractivation activity (By similarity). Interacts with THBS4 (By similarity). Interacts (via the EGF-like repeat region) with CCN3 (via CTCK domain) (By similarity). Interacts (via EGF-like domains) with DLL4 (via N-terminal DSL and MNNL domains) (PubMed:25700513). Interacts with ZMIZ1 (By similarity). Interacts (via NICD domain) with MEGF10 (via the cytoplasmic domain). Interacts with DLL1 and JAG1 (By similarity). Interacts (via NICD domain) with PRAG1 (By similarity). Forms a complex with PRAG1, N1ICD and MAML1, in a MAML1-dependent manner (By similarity). Interacts (via transmembrane region) with PSEN1; the interaction is direct (By similarity).
Heterodimer of a C-terminal fragment N(TM) and an N-terminal fragment N(EC) which are probably linked by disulfide bonds. Interacts with DNER, DTX1, DTX2 and RBPJ/RBPSUH. Also interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH1. Notch 1 intracellular domain interacts with SNW1; the interaction involves multimerized NOTCH1 NICD and is implicated in a formation of an intermediate preactivation complex which associates with DNA-bound CBF-1/RBPJ. The activated membrane-bound form interacts with AAK1 which promotes NOTCH1 stabilization. Forms a trimeric complex with FBXW7 and SGK1. Interacts with HIF1AN. HIF1AN negatively regulates the function of notch intracellular domain (NICD), accelerating myogenic differentiation. Interacts (via NICD) with SNAI1 (via zinc fingers); the interaction induces SNAI1 degradation via MDM2-mediated ubiquitination and inhibits SNAI1-induced cell invasion. Interacts (via NICD) with MDM2A. Interacts (via NICD) with BCL6; the interaction decreases MAML1 recruitment by NOTCH1 NICD on target genes DNA and inhibits NOTCH1 transcractivation activity (By similarity). Interacts with THBS4 (By similarity). Interacts (via the EGF-like repeat region) with CCN3 (via CTCK domain). Interacts (via EGF-like domains) with DLL4 (via N-terminal DSL and MNNL domains). Interacts with ZMIZ1. Interacts (via NICD domain) with MEGF10 (via the cytoplasmic domain). Interacts with DLL1 and JAG1 (By similarity). Interacts (via NICD domain) with PRAG1 (By similarity). Forms a complex with PRAG1, N1ICD and MAML1, in a MAML1-dependent manner (By similarity). Interacts (via transmembrane region) with PSEN1; the interaction is direct (By similarity).
Heterodimer of a C-terminal fragment N(TM) and an N-terminal fragment N(EC) which are probably linked by disulfide bonds. Interacts with DNER, DTX1, DTX2 and RBPJ/RBPSUH. Also interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH1 (PubMed:11101851, PubMed:12370315). The NOTCH1 intracellular domain interacts with SNW1; the interaction involves multimerized NOTCH1 NICD and is implicated in a formation of an intermediate preactivation complex which associates with DNA-bound CBF-1/RBPJ (PubMed:10713164). The activated membrane-bound form interacts with AAK1 which promotes NOTCH1 stabilization. Forms a trimeric complex with FBXW7 and SGK1. Interacts with HIF1AN. HIF1AN negatively regulates the function of notch intracellular domain (NICD), accelerating myogenic differentiation (PubMed:17573339). Interacts (via NICD) with SNAI1 (via zinc fingers); the interaction induces SNAI1 degradation via MDM2-mediated ubiquitination and inhibits SNAI1-induced cell invasion. Interacts (via NICD) with MDM2A. Interacts (via NICD) with BCL6; the interaction decreases MAML1 recruitment by NOTCH1 NICD on target genes DNA and inhibits NOTCH1 transcractivation activity. Interacts with THBS4 (By similarity). Interacts (via the EGF-like repeat region) with CCN3 (via CTCK domain) (PubMed:12050162). Interacts (via EGF-like domains) with DLL4 (via N-terminal DSL and MNNL domains) (By similarity). Interacts with ZMIZ1. Interacts (via NICD domain) with MEGF10 (via the cytoplasmic domain). Interacts with DLL1 and JAG1 (By similarity). Interacts (via NICD domain) with PRAG1 (By similarity). Forms a complex with PRAG1, N1ICD and MAML1, in a MAML1-dependent manner (By similarity). Interacts (via transmembrane region) with PSEN1; the interaction is direct (PubMed:30598546).
Heterodimer of a C-terminal fragment N(TM) and a N-terminal fragment N(EC) which are probably linked by disulfide bonds (By similarity). Interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH4.
Heterodimer of a C-terminal fragment N(TM) and a N-terminal fragment N(EC) which are probably linked by disulfide bonds. Interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH4.
Forms a ternary complex with nrarp and rbpj/suh.
Heterodimer of a C-terminal fragment N(TM) and an N-terminal fragment N(EC) which are probably linked by disulfide bonds (By similarity). Interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH2. Interacts with RELA/p65 (By similarity). Interacts with HIF1AN. Interacts (via ANK repeats) with TCIM, the interaction inhibits the nuclear translocation of NOTCH2 N2ICD (PubMed:25985737). Interacts with CUL1, RBX1, SKP1 and FBXW7 that are SCF(FBXW7) E3 ubiquitin-protein ligase complex components (PubMed:29149593). Interacts with MINAR1; this interaction increases MINAR1 stability and function (PubMed:29329397). Interacts with NOTCH2NL (NOTCH2NLA, NOTCH2NLB and/or NOTCH2NLC); leading to enhance Notch signaling pathway in a non-cell-autonomous manner (PubMed:29856954). Interacts with MDK; this interaction mediates a nuclear accumulation of NOTCH2 and therefore activation of NOTCH2 signaling leading to interaction between HES1 and STAT3 (PubMed:18469519).
Interacts with sel-10.
Interacts with PSMA1 (By similarity). Heterodimer of a C-terminal fragment N(TM) and a N-terminal fragment N(EC) which are probably linked by disulfide bonds. Interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH3. Interacts with HIF1AN.
Heterodimer of a C-terminal fragment N(TM) and an N-terminal fragment N(EC) which are probably linked by disulfide bonds. Interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH2. Interacts with RELA/p65. Interacts with HIF1AN. Interacts (via ANK repeats) with TCIM, the interaction inhibits the nuclear translocation of NOTCH2 N2ICD (By similarity). Interacts with CUL1, RBX1, SKP1 and FBXW7 that are SCF(FBXW7) E3 ubiquitin-protein ligase complex components. Interacts with MINAR1; this interaction increases MINAR1 stability and function (By similarity). Interacts with MDK; this interaction mediates a nuclear accumulation of NOTCH2 and therefore activation of NOTCH2 signaling leading to interaction between HES1 and STAT3 (By similarity).
Heterodimer of a C-terminal fragment N(TM) and an N-terminal fragment N(EC) which are probably linked by disulfide bonds (By similarity). Interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH2. Interacts with RELA/p65 (By similarity). Interacts with HIF1AN. Interacts (via ANK repeats) with TCIM, the interaction inhibits the nuclear translocation of NOTCH2 N2ICD (By similarity). Interacts with CUL1, RBX1, SKP1 and FBXW7 that are SCF(FBXW7) E3 ubiquitin-protein ligase complex components.Interacts with MINAR1; this interaction increases MINAR1 stability and function (By similarity). Interacts with MDK; this interaction mediates a nuclear accumulation of NOTCH2 and therefore activation of NOTCH2 signaling leading to interaction between HES1 and STAT3 (By similarity).
Heterodimer of a C-terminal fragment N(TM) and a N-terminal fragment N(EC) which are probably linked by disulfide bonds. Interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH3. Interacts with PSMA1 (By similarity). Interacts with HIF1AN (By similarity).
Homotetramer.
Heterodimer of a C-terminal fragment N(TM) and a N-terminal fragment N(EC) which are probably linked by disulfide bonds (By similarity). Interacts with MAML1, MAML2 and MAML3 which act as transcriptional coactivators for NOTCH3. Interacts with PSMA1. Interacts with HIF1AN.
Interacts with NOTCH2 and NOTCH3 (By similarity). Interacts with NOTCH1 (in the presence of calcium ions) (PubMed:18660822).
Homomer. Interacts with Su(H) when activated. Interacts with Dx via its ANK repeats. Interacts with Dl via the EGF repeats and the Dl EGF repeats. Interacts with Nedd4 and Su(dx). Interacts with O-fut1; the interaction glycosylates N and transports N to early endosomes. Interacts with Akap200; the interaction stabilizes N/Notch protein levels by preventing Cbl-mediated ubiquitination and subsequent lysosomal degradation of N/Notch (PubMed:29309414).
Interacts with NOTCH1, NOTCH2 and NOTCH3.
Interacts with NOTCH1 (PubMed:28089369). Interacts with NOTCH2 and NOTCH3 (By similarity).
Component of the SAC complex, a complex composed of crb, Patj and sdt (PubMed:11740560, PubMed:10102271, PubMed:11076972). May interact with the par-6 complex, which is composed of par-6, baz and aPKC, via its interaction with Patj (PubMed:12900452, PubMed:10102271, PubMed:11076972). Interacts with other proteins with Patj and sdt via its short cytoplasmic tail (PubMed:11740560). Component of the CGX complex composed of crb, galla (galla-1 or galla-2) and Xpd (PubMed:25065591). Able to interact independently (via intracellular domain) with galla-1, galla-2 and Xpd (PubMed:25065591). Interacts with apn (PubMed:30645584).
Homodimer (PubMed:12794186). Interacts with TJP1 (PubMed:24715457). Interacts with MMP14; inhibits DLL1-induced Notch signaling (PubMed:21572390). Interacts with MAGI1 (via PDZ domain); forms a complex with CTNNB1 and CDH2 and promotes recruitment to the adherens junction and stabilization on the cell surface (PubMed:15908431). Interacts with PSEN1; undergoes a presenilin-dependent gamma-secretase cleavage that releases a Dll1-intracellular form (PubMed:12794186). Interacts with MFAP5 (PubMed:15788413). Interacts with MIB1 (PubMed:21985982). Interacts with NEURL1B; leads to ubiquitination (PubMed:17003037, PubMed:19723503). Interacts with NEURL1 (PubMed:19723503). Interacts with SYNJ2BP; enhances DLL1 protein stability, and promotes Notch signaling in endothelial cells (By similarity). Interacts with MAGI1, MAGI2, MAGI3 and MPDZ (By similarity). Interacts (via ubiquitin) with EPN1 (via IUM domain); binding with NOTCH1 attached to neighboring cell, promotes ligand ubiquitination and EPN1 interaction, leading to NECD transendocytosis and Notch signaling. Interacts with NOTCH1 (By similarity).
In photoreceptor cells, forms a complex with MPDZ, MPP4 and MPP5.
Heterodimer and heterotetramer with AXL.
Homodimer. Interacts with TJP1. Interacts with MAGI1 (via PDZ domain); forms a complex with CTNNB1 and CDH2 and promotes recruitment to the adherens junction and stabilization on the cell surface. Interacts with PSEN1; undergoes a presenilin-dependent gamma-secretase cleavage that releases a Dll1-intracellular form. Interacts with MFAP5. Interacts with MIB1. Interacts with NEURL1B; leads to ubiquitination. Interacts with NEURL1 (By similarity). Interacts with SYNJ2BP; enhances DLL1 protein stability, and promotes Notch signaling in endothelial cells. Interacts with MAGI1, MAGI2, MAGI3 and MPDZ (By similarity). Interacts (via ubiquitin) with EPN1 (via IUM domain); binding with NOTCH1 attached to neighboring cell, promotes ligand ubiquitination and EPN1 interaction, leading to NECD transendocytosis and Notch signaling (PubMed:22658936). Interacts with NOTCH1 (PubMed:28089369).
Interacts with mib.
Interacts with N via the EGF repeats and the N EGF repeats.
Interacts with CHID1.
Interacts with heparin, alpha-M/beta-2 integrin (ITGAM and ITGB2), and thymosin beta 4 (TMSB4X) (By similarity). Interacts with GULP1. Associates with clathrin and adapter protein AP-2; in liver sinusoidal endothelial cells (LSECs).
Homopentamer; disulfide-linked. Interacts with PTBP3. Interacts with NOTCH1 (By similarity). Interacts (via EGF-like 3; calcium-binding domain) with ATF6 and facilitates its processing, activation and nuclear translocation.
Miscellaneous
Mutations in TLD lead to a partial transformation of dorsal ectoderm into ventral ectoderm.
Although the protein is conserved in Drosophila, the gene encoding the orthologous protein is inactive in rodents.
When exogenously expressed, the C-terminal part is nuclear, phosphorylated, and acts as an insulin-responsive transcriptional activator.
Separation of neuroblasts from the ectoderm into the inner part of embryo is one of the first steps of CNS development in insects, this process is under control of the neurogenic genes.
Notch and Serrate may interact at the protein level, it is conceivable that the Serrate and Delta proteins may compete for binding with the Notch protein.
Similarity
Belongs to the DMBT1 family.
Belongs to the NOTCH family.
Belongs to the EYS family.
Belongs to the Crumbs protein family.
Belongs to the thrombospondin family.
Keywords
Calcium   Cell membrane   Complete proteome   Disulfide bond   EGF-like domain   Glycoprotein   Membrane   Metal-binding   Protein transport   Reference proteome   Repeat   Signal   Transport   Cholesterol metabolism   Cleavage on pair of basic residues   Cobalamin   Cobalt   Direct protein sequencing   Endosome   Lipid metabolism   Lysosome   Phosphoprotein   Steroid metabolism   Sterol metabolism   Coated pit   3D-structure   Disease mutation   Endocytosis   Polymorphism   Receptor   Secreted   Developmental protein   Differentiation   Hydrolase   Metalloprotease   Protease   Zinc   Zymogen   Methylation   Alternative splicing   Atrial septal defect   Chondrogenesis   Cytokine   Extracellular matrix   Golgi apparatus   Growth factor   Osteogenesis   Osteogenesis imperfecta   Cytoplasmic vesicle   Transmembrane   Transmembrane helix   Activator   Angiogenesis   ANK repeat   Hydroxylation   Isopeptide bond   Notch signaling pathway   Nucleus   Transcription   Transcription regulation   Ubl conjugation   Triplet repeat expansion   Proto-oncogene   Cytoplasm   Cell projection   Cytoskeleton   Sensory transduction   Vision   Retinitis pigmentosa   Gastrulation   Deafness   Neurogenesis   Oogenesis   Sushi   Cell cycle   Cell division   Mitosis   Cell junction   Gamma-carboxyglutamic acid   Growth regulation   Host-virus interaction   Cell adhesion   Inflammatory response   Laminin EGF-like domain   Hyaluronic acid   Endoplasmic reticulum   Mitogen   Sarcoplasmic reticulum   Tissue remodeling   Unfolded protein response  
Feature
chain  Cubilin homolog
propeptide  Removed in mature form
sequence variant  In dbSNP:rs12259370.
splice variant  In isoform 2.
EC Number
3.4.24.-
3.4.24.19
Pubmed
10731132    12537572    12537569    23264686    10552972    9478979    + More
9153271    9691015    10400683    10811843    11805171    12724130    15616221    16641100    20237569    19468303    11856751    10766831    11278724    14983511    15342463    19349973    21183079    9572993    15164054    10371504    11717447    11606717    14576052    17124247    10080186    10887099    16959974    21355061    21248752    23114252    9851916    12754521    17761667    9520331    10479448    15489334    11313359    24129315    10231032    10896944    18824173    18830233    12464431    10940628    9395394    10375503    8661043    16141072    10331975    8174772    20181949    8643539    3201241    9500680    7798260    14702039    11283002    12637569    14759258    22482805    22052668    25402547    8742698    10679193    7876332    7537458    8543783    9247472    9688648    11152281    12082154    12884308    15146979    15292166    15452149    15987769    17983803    18202109    1840509    7600963    8449489    7956822    12123574    12807718    1426644    8440332    1425352    9653148    10437788    8486742    18299578    9384671    10882062    10882063    11518718    11459941    11226752    12050162    15019995    15240571    15965470    18628966    21464124    21757702    23160044    23886940    23615612    25038227    28089369    28498977    30127001    15802643    17573339    1764995    15057822    11182080    1295745    11438922    25700513    21804562    10734111    15164053    1831692    10079256    9590294    10713164    11101851    12370315    16025100    18669648    20616313    22128911    21147854    21245387    24226769    25547411    26522984    12795601    15576031    16011479    16530044    28439555    30598546    25132448    20431018    9168133    9693032    14574404    1312643    9150355    8681805    14656967    10233982    11344305    2402639    11485984    16710414    1303260    9244302    17081983    18469519    19690332    20068231    21681853    21378989    21378985    23186163    25985737    29149593    29856954    29329397    17401372    16773578    21793104    21712856    23389697    3419531    7906398    3000611    9389650    8297791    7918097    8917536    10393120    7609614    18710934    19144319    21949356    11577080    22673903    23594743    27737822    28378834    30052645    18976725    18836446    12975309    20696082    27846257    21069908    20333770    26593283    2514273    3498216    2784773    2060714    15659374    8878478    15057824    17292860    25394726    9388399    10227618    10371548    10854111    11058919    11102981    10802807    11559313    11755616    11810186    12146805    12136071    12589106    12810003    15229130    15364702    15378071    15350543    15300988    16009764    15818833    18273901    23731542    24000151    15851977    25557779    25557780    9268641    9207788    9462510    10329626    11780052    8955070    9207787    10978356    21269460    18660822    19586525    9585603    10220506    10533065    11058898    11152664    11157803    11139247    11180599    12022040    12297837    12442286    12649809    12497640    15712272    16575836    23801938    20437614    3935325    3097517    10731137    3037327    2981631    2780284    8162848    7671825    10206646    10206647    10935637    11719214    11799064    12369105    12909620    15620649    15620650    17329366    18243100    18342578    18327897    20152183    21262215    23056424    27268051    27151950    28899667    29309414    14573873    10551863    10556292    9341252    9486542    9315665    7697721    22072575    23001562    26496195    27870829    26802325    10662552    8948600    2758466    1881436    8350921    8156602    9861048    16319922    22820175    22278922    24332851    28853436    15815621    15194686    12665856    15162516    2344615    3107986    10102271    11076972    11740560    12900452    17893096    25065591    30645584    2125287    1840519    15829515    15760269    7671806    21572390    12794186    10958687    15146182    15788413    15908431    16495313    17003037    17194759    18997111    17960184    18676613    19723503    19144989    19389377    19217325    19562077    20081190    21985982    21238454    21915337    22282195    22096075    22015720    22940113    22529374    23806616    23699523    23688253    23695674    24715457    25220152    24449764    26114479    11744384    14684155    11850625    12915475    15316081    8336730    15108283    15057823    7854420    7867073    9326368    8939948    9326369    12364394    18840707    21501828    23084921    17005688    26091039    8621659    16362042    12036964    22658936    9425133    9425132    10074451    10572043    15013799    15068793    15659486    17139625    9203139    12361969    11100729    12530964    10585570    16453806    3149249    15020426    2128477    11829752    12077138    9039502    12168954    16641997    16357325    19159218    24275569    16206243    17974005    12747765    11062057    22171320    12473645    14598175    15572036    17242355    18230608    8350346    7852353    19441079    22682248    23287452    23892609    22011848   
EMBL
AE014298    AY084200    AAL89938.1    AF137068    AF022247    AL773538    + More
AL928807    AF197159    AF034611    EF444970    AC067747    AL365215    AL596445    AL731551    Z74046    Z74473    Y09661    AF073526    BC132537    AF059516    AB023149    AL138765    AL136181    AL391136    BC013871    BC112341    BC112366    BC113577    U91963    AF282732    CH471056    BC016922    BC136429    BC136430    AF393242    AJ012462    AF027596    U34042    AK080919    AK139103    L24755    AC122268    BC066062    U50330    M22488    Y08723    Y08724    Y08725    L35278    L35279    AK291620    CH471080    BC136679    U37438    AB005909    BC049835    M76976    U04239    AE014297    Z11886    AF508809    AB100603    AL732541    CH466542    BC138441    BC138442    L02613    X68278    AK154528    AK157475    AJ238029    X82562    X57405    AABR06021907    AABR06021908    CH474001    JH001398    AF308602    AL592301    AL354671    M73980    AB209873    AAMC01043423    AAMC01043424    AAMC01043425    AAMC01043426    BC133053    D63395    D86566    U95299    U89335    AL662884    BX284686    BX284927    CR812478    CR933878    AB023961    AB024520    AB024578    M80456    U43691    AF030001    CT009767    AB016771    AB016772    AB016773    AB016774    M33874    AF308601    AF315356    AL359752    AL512503    AL596222    U77493    M12069    Z14092    X69088    X74760    D32210    AC154173    AC164091    CH466620    X68279    U31881    M93661    BX005106    BX323836    CR456624    CU570696    AF164486    FM209056    FJ416331    AY358133    AL050329    AL078597    AL109612    AL109922    AL132767    AL133322    AL137007    AL353153    AL353669    AL354719    AL354913    AL355357    AL356454    AL357375    AL365217    AL450319    AL450324    AL450394    AL589916    AL590546    AL590784    AL603767    BC133011    BC133013    AF229451    NDHI03003297    CR860424    AF229448    L08692    X17530    M17421    X17533    U97669    AF058900    AF058881    AF058882    AF058883    AF058884    AF058885    AF058886    AF058887    AF058888    AF058889    AF058890    AF058891    AF058892    AF058893    AF058894    AF058895    AF058896    AF058897    AF058898    AF058899    AC004257    AC004663    AY720432    AK123000    AK126775    AL445489    AL365504    DQ426866    AF003837    U73936    AF028593    U61276    AK302554    AL035456    BC126205    BC126207    U77720    M16152    M16153    M16149    M16150    M16151    K03508    M13689    K03507    AL035436    AL035395    M16025    M12175    AF171092    BC058675    AF038572    AC160929    AF010137    Y14495    L38483    AL805959    BC043114    BC062128    AF020201    AF003521    AF029778    AF029779    AF111170    Y14330    U70050    M25580    BX284603    Z29116    AC005237    AC093585    AC104809    AK074062    AK074075    AF439717    AF439718    BC027939    AY169783    AJ584850    BC145886    AK032805    AABR03068156    AABR03069106    AABR03069488    AABR03071665    AABR03072503    AF439715    AF439719    M33753    AY118509    X05144    M35759    X56811    X80903    AY497019    CH466630    BC057400    BC065063    AF406641    AY450552    AF492496    AK044345    AK044704    AC116810    AC138741    AL606536    CH466520    L13720    AY256843    AY256830    AY256831    AY256832    AY256833    AY256834    AY256835    AY256836    AY256837    AY256838    AY256839    AY256840    AY256841    AY256842    AK092028    AK122969    AK126533    AK290803    EF631974    BX072579    BC038984    AY170372    BK001240    U78889    AF030031    BC075742    AABR03040659    AABR03041327    AABR03041522    AABR03042206    AABR03044351    AABR03044745    AABR03045322    Y11760    AF426384    AF146429    X06289    Y00222    AY437145    AY437140    AY437141    AY437142    AY437143    AY437144    AY437151    AY437146    AY437147    AY437148    AY437149    AY437150    AY437157    AY437152    AY437153    AY437154    AY437155    AY437156    AY437163    AY437158    AY437159    AY437160    AY437161    AY437162    AY437169    AY437164    AY437165    AY437166    AY437167    AY437168    AY437175    AY437170    AY437171    AY437172    AY437173    AY437174    AY437181    AY437176    AY437177    AY437178    AY437179    AY437180    AY437187    AY437182    AY437183    AY437184    AY437185    AY437186    AY437193    AY437188    AY437189    AY437190    AY437191    AY437192    AY437199    AY437194    AY437195    AY437196    AY437197    AY437198    AY437205    AY437200    AY437201    AY437202    AY437203    AY437204    AY437211    AY437206    AY437207    AY437208    AY437209    AY437210    AY437217    AY437212    AY437213    AY437214    AY437215    AY437216    AY437223    AY437218    AY437219    AY437220    AY437221    AY437222    AY437229    AY437224    AY437225    AY437226    AY437227    AY437228    AY437235    AY437230    AY437231    AY437232    AY437233    AY437234    AY438104    AY438105    AY438106    AY438107    AY438108    AY438109    AY438110    AY438111    AY438112    AY438113    AY438114    AY438115    AY438116    AY438117    AY438118    AY438119    AY438120    AY438121    AY438122    AY438123    AY438124    AY438125    AY438126    AY438127    AY438128    AY438129    AY438130    AY438131    AY438132    AY438133    AY438134    AY438135    AY438136    AY438137    AY438138    AY438139    AY438140    AY438141    AY438147    AY438148    AY438149    AY438150    AY438151    AY438152    AY438153    AY438154    AY438155    AY438156    AY438157    AY438158    AY438159    AY438160    AY438161    AY438162    AY438163    AY438164    AY438165    AY438166    AY438167    AY438168    AY438169    AY438170    AY438171    AY438172    AY438173    AY438174    AY438175    AY438176    AY438177    AY438178    AY438179    AY438180    AY438181    AY438182    AY438183    AY438184    AY438185    AY438186    AY438187    AY438188    AY438189    AY438190    AY438191    AY438192    AY438193    AY438194    AY438195    AY438196    AY438197    AY438198    AY438199    AY438200    AY438201    AY438202    BK004004    BT003267    AY061269    X05140    AJ275213    AB052956    AB052957    D87433    AC006208    AC112215    BC150250    BAA13377.2    CAB61827.1    AJ619977    AY916667    AK023591    AK075235    AK027870    AL158158    AL354982    AL592463    BC030816    BX537918    BX538049    AF308289    AF364951    AK034522    AAL91684.2    Z19585    AK313587    AY566253    BC050456   
Pfam
PF00008   EGF        + More
PF00431   CUB
PF07645   EGF_CA
PF12661   hEGF
PF12947   EGF_3
PF01400   Astacin
PF00530   SRCR
PF00100   Zona_pellucida
PF00066   Notch
PF11936   DUF3454
PF12796   Ank_2
PF07684   NODP
PF06816   NOD
PF00023   Ank
PF02210   Laminin_G_2
PF07657   MNNL
PF01414   DSL
PF01382   Avidin
PF06119   NIDO
PF00041   fn3
PF00054   Laminin_G_1
PF12662   cEGF
PF00594   Gla
PF00092   VWA
PF00354   Pentaxin
PF02494   HYR
PF00084   Sushi
PF07699   Ephrin_rec_like
PF02469   Fasciclin
PF00193   Xlink
PF05735   TSP_C
PF02412   TSP_3
PF11598   COMP
Interpro
IPR009030   Growth_fac_rcpt_cys_sf        + More
IPR001881   EGF-like_Ca-bd_dom       
IPR018097   EGF_Ca-bd_CS       
IPR000859   CUB_dom       
IPR035914   Sperma_CUB_dom_sf       
IPR000152   EGF-type_Asp/Asn_hydroxyl_site       
IPR013032   EGF-like_CS       
IPR000742   EGF-like_dom       
IPR024731   EGF_dom       
IPR034036   ZnMP_TLD/BMP1       
IPR015446   BMP_1/tolloid-like       
IPR001506   Peptidase_M12A       
IPR024079   MetalloPept_cat_dom_sf       
IPR006026   Peptidase_Metallo       
IPR029837   BMP-1       
IPR001507   ZP_dom       
IPR017977   ZP_dom_CS       
IPR036772   SRCR-like_dom_sf       
IPR001190   SRCR       
IPR017448   SRCR-like_dom       
IPR036770   Ankyrin_rpt-contain_sf       
IPR010660   Notch_NOD_dom       
IPR022362   Notch_1       
IPR035993   Notch-like_dom_sf       
IPR011656   Notch_NODP_dom       
IPR020683   Ankyrin_rpt-contain_dom       
IPR008297   Notch       
IPR000800   Notch_dom       
IPR002110   Ankyrin_rpt       
IPR024600   DUF3454_notch       
IPR022355   Notch_4       
IPR022336   Notch_2       
IPR022331   Notch_3       
IPR001791   Laminin_G       
IPR013320   ConA-like_dom_sf       
IPR026219   Jagged/Serrate       
IPR001007   VWF_dom       
IPR011651   Notch_ligand_N       
IPR001774   DSL       
IPR036896   Avidin-like_sf       
IPR005468   Avidin/str       
IPR005469   Avidin       
IPR017889   Avidin-like_CS       
IPR033108   Jag2       
IPR036116   FN3_sf       
IPR035976   Sushi/SCR/CCP_sf       
IPR013783   Ig-like_fold       
IPR003961   FN3_dom       
IPR000436   Sushi_SCR_CCP_dom       
IPR003886   NIDO_dom       
IPR017857   Coagulation_fac-like_Gla_dom       
IPR000294   GLA_domain       
IPR026823   cEGF       
IPR035972   GLA-like_dom_SF       
IPR036465   vWFA_dom_sf       
IPR002035   VWF_A       
IPR001759   Pentraxin-related       
IPR003410   HYR_dom       
IPR011641   Tyr-kin_ephrin_A/B_rcpt-like       
IPR000782   FAS1_domain       
IPR036378   FAS1_dom_sf       
IPR000538   Link_dom       
IPR016187   CTDL_fold       
IPR016186   C-type_lectin-like/link_sf       
IPR002049   Laminin_EGF       
IPR028974   TSP_type-3_rpt       
IPR003367   Thrombospondin_3-like_rpt       
IPR024665   Thbs/COMP_coiled-coil       
IPR017897   Thrombospondin_3_rpt       
IPR008859   Thrombospondin_C       
SUPFAM
SSF57184   SSF57184        + More
SSF49854   SSF49854       
SSF56487   SSF56487       
SSF90193   SSF90193       
SSF48403   SSF48403       
SSF49899   SSF49899       
SSF50876   SSF50876       
SSF57535   SSF57535       
SSF49265   SSF49265       
SSF57630   SSF57630       
SSF53300   SSF53300       
SSF56436   SSF56436       
SSF82153   SSF82153       
SSF103647   SSF103647       
PDB
6GJE     E-value=0,     Score=2525

Ontologies

GO
GO:0097206   GO:0015031   GO:0097017   GO:0005886   GO:0005509   GO:0010008   GO:0016324   GO:0008203   GO:0031419   GO:0008144   GO:0031526   GO:0005765   GO:0006766   GO:0020028   GO:0001701   GO:0032991   GO:0030492   GO:0006898   GO:0038024   GO:0070207   GO:0007584   GO:0005905   GO:0043202   GO:0042802   GO:0016020   GO:0030666   GO:0005798   GO:0015889   GO:0030135   GO:0042366   GO:0038023   GO:0005737   GO:0045177   GO:0042953   GO:0005794   GO:0005768   GO:0030139   GO:0009617   GO:0070062   GO:0005783   GO:0042803   GO:0005903   GO:0009235   GO:0031232   GO:0001894   GO:0005829   GO:0034384   GO:0042359   GO:0005576   GO:0006629   GO:0007275   GO:0008270   GO:0004222   GO:0030154   GO:0048632   GO:0022617   GO:0001501   GO:0036342   GO:0035124   GO:0008233   GO:0001707   GO:0008237   GO:0035162   GO:0006508   GO:0009953   GO:0001568   GO:0001885   GO:0048264   GO:0030513   GO:0005518   GO:0005125   GO:0062023   GO:0005615   GO:0061036   GO:0051216   GO:0001503   GO:0031982   GO:0008083   GO:0001502   GO:0034380   GO:0005044   GO:0042589   GO:0050830   GO:0035375   GO:0030658   GO:0001833   GO:0050829   GO:0030670   GO:0009897   GO:0001824   GO:0016021   GO:0030858   GO:0031012   GO:0019898   GO:0032927   GO:0017015   GO:0007378   GO:0007313   GO:0008586   GO:0009880   GO:0016485   GO:0021915   GO:0035924   GO:0005112   GO:0003203   GO:0061384   GO:0005856   GO:0001889   GO:0043565   GO:0003162   GO:0010832   GO:0045668   GO:0045687   GO:0007050   GO:0000139   GO:0048708   GO:0030334   GO:0050434   GO:0045747   GO:0010628   GO:0060253   GO:0030326   GO:1903849   GO:0045893   GO:0008593   GO:2000737   GO:2001027   GO:0055008   GO:0060271   GO:0070374   GO:0045596   GO:0030514   GO:0003182   GO:0070986   GO:0072044   GO:0007492   GO:0048711   GO:0004888   GO:0003181   GO:0000978   GO:0060317   GO:0045618   GO:0001228   GO:0003198   GO:0005789   GO:0048845   GO:0003209   GO:0045607   GO:0009912   GO:0003344   GO:0048663   GO:0060843   GO:0090051   GO:0031069   GO:0045967   GO:0045892   GO:0048103   GO:0060982   GO:0061344   GO:0010001   GO:0003252   GO:0001726   GO:0060548   GO:0001947   GO:0061314   GO:0007507   GO:0071372   GO:0005654   GO:0008284   GO:0002052   GO:0032496   GO:0030182   GO:0002040   GO:0014031   GO:0003160   GO:0032495   GO:0021515   GO:0042127   GO:0072017   GO:0045608   GO:0030900   GO:0031410   GO:0035914   GO:0048873   GO:0003241   GO:0005634   GO:0007386   GO:0007221   GO:0003219   GO:0060528   GO:0060740   GO:0062043   GO:0008285   GO:0071944   GO:0002437   GO:0060956   GO:0045165   GO:0030216   GO:1901201   GO:0061419   GO:0008544   GO:0005887   GO:0010629   GO:0003157   GO:0043086   GO:0014807   GO:0003332   GO:0035148   GO:0003222   GO:0050767   GO:0050679   GO:0060768   GO:0045665   GO:0003180   GO:0043065   GO:0046579   GO:1902263   GO:0030027   GO:2000974   GO:0001837   GO:0043235   GO:0060411   GO:0046982   GO:0003256   GO:0035116   GO:0006959   GO:0060979   GO:0045955   GO:0046533   GO:0003151   GO:0045944   GO:0005912   GO:0060948   GO:0010718   GO:0003270   GO:0042246   GO:0072602   GO:0003208   GO:0031960   GO:0003192   GO:0007219   GO:0010614   GO:0003207   GO:0031100   GO:0003682   GO:0007409   GO:0003197   GO:2000811   GO:0070168   GO:0007283   GO:0030324   GO:0001708   GO:0007440   GO:0003700   GO:0090090   GO:0019899   GO:0003169   GO:0030335   GO:0045662   GO:0004857   GO:0010468   GO:0003213   GO:1902339   GO:0002051   GO:0046427   GO:0048754   GO:0060038   GO:0009986   GO:0001669   GO:0003184   GO:0060412   GO:0030279   GO:0000122   GO:0010812   GO:0060842   GO:0050678   GO:0060045   GO:0003264   GO:0072144   GO:0002193   GO:0120163   GO:0045603   GO:0003214   GO:0007368   GO:0003273   GO:0045070   GO:0048709   GO:1901189   GO:0048715   GO:0031490   GO:0006357   GO:0050768   GO:0007420   GO:0050793   GO:0005796   GO:0006355   GO:0001525   GO:0097150   GO:0006367   GO:0006955   GO:0045602   GO:0001886   GO:0001944   GO:0001569   GO:0030097   GO:0035278   GO:0045746   GO:0042060   GO:0001709   GO:0001763   GO:0030879   GO:0070613   GO:0045446   GO:0045766   GO:0032880   GO:0010838   GO:0006915   GO:0019827   GO:0060413   GO:0007399   GO:2001204   GO:0002315   GO:0009887   GO:0043066   GO:2000249   GO:0046849   GO:0048337   GO:0042661   GO:0045168   GO:0018991   GO:0043054   GO:0040028   GO:0001085   GO:0090575   GO:0040025   GO:0002119   GO:0042659   GO:0021986   GO:0001756   GO:0021531   GO:0001840   GO:0048699   GO:0048259   GO:0031016   GO:0009952   GO:0048936   GO:0031017   GO:0021514   GO:0042663   GO:0035907   GO:0021523   GO:0055016   GO:0002244   GO:0048844   GO:0072104   GO:0015629   GO:0048661   GO:0072015   GO:0005929   GO:0072014   GO:0035264   GO:0001890   GO:1990705   GO:0045672   GO:0035622   GO:0043011   GO:0060674   GO:0051059   GO:0072576   GO:0042742   GO:0061073   GO:0002011   GO:0072574   GO:0007015   GO:0033165   GO:0050896   GO:0007601   GO:0046549   GO:0035845   GO:0045494   GO:0005815   GO:0050908   GO:0001750   GO:0043403   GO:0030878   GO:0042472   GO:0031101   GO:0048752   GO:1904888   GO:0060325   GO:0032474   GO:0060351   GO:0060117   GO:0060872   GO:0060218   GO:0032579   GO:0045296   GO:0055111   GO:0010470   GO:0072358   GO:0010951   GO:0014028   GO:0007157   GO:0045197   GO:0019828   GO:0045199   GO:0044877   GO:0045599   GO:0001953   GO:0061156   GO:0035909   GO:0061444   GO:0030336   GO:0045639   GO:0005543   GO:0045669   GO:0072006   GO:0061309   GO:0022408   GO:0005198   GO:0001974   GO:0003215   GO:0045445   GO:0002456   GO:0042491   GO:0072070   GO:0035204   GO:0048749   GO:1900087   GO:0008356   GO:0008347   GO:0043525   GO:0030720   GO:0060250   GO:0007519   GO:0030713   GO:0035003   GO:0022416   GO:0036099   GO:0007398   GO:0045466   GO:0007314   GO:0016360   GO:0050877   GO:0007473   GO:2000035   GO:0007298   GO:0005915   GO:2000048   GO:0005769   GO:0048665   GO:0007451   GO:0035153   GO:0061382   GO:0060571   GO:0007450   GO:0007346   GO:0007422   GO:0048052   GO:0008045   GO:0035172   GO:0007474   GO:0042691   GO:0048863   GO:0046666   GO:0035214   GO:0042689   GO:0008587   GO:0007405   GO:0046667   GO:0060289   GO:0046329   GO:0016348   GO:0042676   GO:0045316   GO:0035222   GO:0001745   GO:0035165   GO:0060288   GO:0048664   GO:0040008   GO:0035171   GO:0048190   GO:0007498   GO:0007464   GO:0036011   GO:0014019   GO:0008407   GO:0042688   GO:0048803   GO:1902692   GO:1990433   GO:0030708   GO:0007297   GO:0002213   GO:0007476   GO:0048542   GO:0046843   GO:0007446   GO:0007400   GO:0009608   GO:0016333   GO:0016330   GO:0007419   GO:0043697   GO:0035167   GO:0007423   GO:0007411   GO:0030718   GO:0007616   GO:0007455   GO:0006110   GO:0046331   GO:0008340   GO:0007403   GO:0009950   GO:0046716   GO:0042067   GO:0036335   GO:0051489   GO:0007391   GO:0007447   GO:0005770   GO:0030707   GO:0042686   GO:0048477   GO:0007478   GO:0061331   GO:0007521   GO:0005788   GO:0045595   GO:0007293   GO:0048018   GO:0043010   GO:0048839   GO:0030155   GO:0030217   GO:0045061   GO:1990134   GO:0042475   GO:0007605   GO:0042492   GO:0016331   GO:0003016   GO:0048471   GO:0001666   GO:0008584   GO:0012505   GO:0043282   GO:0043055   GO:2000648   GO:1905938   GO:0044214   GO:0016328   GO:0003713   GO:1905936   GO:0007160   GO:0035332   GO:0016332   GO:0003383   GO:0061024   GO:0005080   GO:0046621   GO:0007163   GO:0106036   GO:0035239   GO:0061336   GO:0007443   GO:0007435   GO:0005819   GO:0046664   GO:0007424   GO:0032435   GO:0035090   GO:0045570   GO:0098813   GO:0016028   GO:0033157   GO:0061541   GO:0016334   GO:0051642   GO:0046665   GO:0034332   GO:0042051   GO:0045186   GO:0030507   GO:0035088   GO:0045176   GO:0050821   GO:0045218   GO:0060438   GO:0051301   GO:0042052   GO:0016327   GO:0035002   GO:0043208   GO:0045179   GO:0035017   GO:0007436   GO:0048100   GO:0030673   GO:0014009   GO:0097110   GO:0097009   GO:0048633   GO:0098773   GO:0035265   GO:1903672   GO:0001757   GO:0009954   GO:0014002   GO:0008217   GO:0007267   GO:0030957   GO:0021510   GO:0021693   GO:0072583   GO:0032693   GO:0034351   GO:0060041   GO:2000726   GO:0097102   GO:1900746   GO:0030857   GO:0045605   GO:0051302   GO:0048630   GO:0060042   GO:0045121   GO:0003323   GO:0045638   GO:0021688   GO:0048631   GO:0045807   GO:0060853   GO:0001917   GO:0005902   GO:0042462   GO:0005913   GO:0007009   GO:0030296   GO:0043027   GO:0046827   GO:0035690   GO:0006468   GO:0085029   GO:0002576   GO:0050711   GO:0007155   GO:0031093   GO:0061098   GO:0043154   GO:0019064   GO:0043687   GO:1900142   GO:0007165   GO:0043491   GO:0016477   GO:0097028   GO:0043433   GO:0070588   GO:0048146   GO:0032148   GO:0001961   GO:0033138   GO:0018105   GO:2000533   GO:0030168   GO:0051897   GO:0019079   GO:2000352   GO:0001764   GO:0070527   GO:0032689   GO:0046718   GO:0005245   GO:0032008   GO:0001786   GO:0001934   GO:0035754   GO:0031589   GO:0050900   GO:2000669   GO:0007167   GO:0072659   GO:0035457   GO:0010934   GO:0006888   GO:0005102   GO:0032720   GO:0046813   GO:0071307   GO:0045860   GO:0043277   GO:0032715   GO:2000270   GO:0044267   GO:0050766   GO:0030971   GO:0010804   GO:0006909   GO:0032825   GO:0030674   GO:0097241   GO:1900165   GO:0009267   GO:0071333   GO:0008283   GO:2000510   GO:0003104   GO:0071363   GO:0021536   GO:0060034   GO:0005938   GO:0014032   GO:0022008   GO:0060113   GO:0030901   GO:0033504   GO:0061056   GO:0048546   GO:1902036   GO:0035469   GO:0003140   GO:0030165   GO:0071910   GO:0048666   GO:0048514   GO:0007475   GO:0048800   GO:0007480   GO:0045931   GO:0005041   GO:0030169   GO:0015035   GO:0006954   GO:0005540   GO:0016525   GO:0006897   GO:0005604   GO:0008201   GO:0034103   GO:0005178   GO:0048771   GO:0071603   GO:0051451   GO:0016529   GO:0050731   GO:0048266   GO:0001938   GO:0090023   GO:0034976   GO:0006986   GO:0051781   GO:0005515   GO:0005840   GO:0006412   GO:0015934   GO:0015914   GO:0046872   GO:0016876   GO:0043039  

Topology

Subcellular location
Cell membrane  
Endosome membrane   Colocalizes with AMN and LRP2 in the endocytotic apparatus of epithelial cells.   With evidence from 1 publications.
Lysosome membrane   Colocalizes with AMN and LRP2 in the endocytotic apparatus of epithelial cells.   With evidence from 1 publications.
Apical cell membrane   Colocalizes with AMN and LRP2 in the endocytotic apparatus of epithelial cells.   With evidence from 1 publications.
Membrane   Colocalizes with AMN and LRP2 in the endocytotic apparatus of epithelial cells.   With evidence from 1 publications.
Coated pit   Colocalizes with AMN and LRP2 in the endocytotic apparatus of epithelial cells.   With evidence from 1 publications.
Endosome   Colocalizes with AMN and LRP2 in the endocytotic apparatus of epithelial cells.   With evidence from 1 publications.
Secreted  
Golgi apparatus  
trans-Golgi network  
Extracellular space  
Extracellular matrix  
Cytoplasmic vesicle  
Secretory vesicle membrane  
Nucleus   Following proteolytical processing NICD is translocated to the nucleus. Nuclear location may require MEGF10.   With evidence from 35 publications.
Cytoplasm   Following proteolytical processing NICD is translocated to the nucleus. Retained at the cytoplasm by TCIM (PubMed:25985737).   With evidence from 26 publications.
Cell projection   Localizes to discrete puncta at, or adjacent to, the photoreceptor connecting cilium (PubMed:27737822, PubMed:30052645). May localize to the cilium axoneme (By similarity). May also be expressed in the interphotoreceptor extracellular matrix (By similarity). Unlike the primate ortholog, does not appear to be expressed in the photoreceptor outer segment (PubMed:27737822).   With evidence from 1 publications.
Cilium   Localizes to discrete puncta at, or adjacent to, the photoreceptor connecting cilium (PubMed:27737822, PubMed:30052645). May localize to the cilium axoneme (By similarity). May also be expressed in the interphotoreceptor extracellular matrix (By similarity). Unlike the primate ortholog, does not appear to be expressed in the photoreceptor outer segment (PubMed:27737822).   With evidence from 1 publications.
Cytoskeleton   Localizes to discrete puncta at, or adjacent to, the photoreceptor connecting cilium (PubMed:27737822, PubMed:30052645). May localize to the cilium axoneme (By similarity). May also be expressed in the interphotoreceptor extracellular matrix (By similarity). Unlike the primate ortholog, does not appear to be expressed in the photoreceptor outer segment (PubMed:27737822).   With evidence from 1 publications.
Cilium axoneme   Localizes to discrete puncta at, or adjacent to, the photoreceptor connecting cilium (PubMed:27737822, PubMed:30052645). May localize to the cilium axoneme (By similarity). May also be expressed in the interphotoreceptor extracellular matrix (By similarity). Unlike the primate ortholog, does not appear to be expressed in the photoreceptor outer segment (PubMed:27737822).   With evidence from 1 publications.
Interphotoreceptor matrix   Localizes to discrete puncta at, or adjacent to, the photoreceptor connecting cilium (PubMed:27737822, PubMed:30052645). May localize to the cilium axoneme (By similarity). May also be expressed in the interphotoreceptor extracellular matrix (By similarity). Unlike the primate ortholog, does not appear to be expressed in the photoreceptor outer segment (PubMed:27737822).   With evidence from 1 publications.
Photoreceptor outer segment   Localizes to discrete puncta at, or adjacent to, the photoreceptor connecting cilium (PubMed:27737822). Highly expressed in cone photoreceptor outer segments (PubMed:27737822). Weakly expressed in rod photoreceptor outer segments (By similarity). May localize to the cilium axoneme (PubMed:27846257). May also be secreted into the interphotoreceptor extracellular matrix (PubMed:27737822).   With evidence from 2 publications.
Microtubule organizing center   Localizes to discrete puncta at, or adjacent to, the photoreceptor connecting cilium (PubMed:27737822). Highly expressed in cone photoreceptor outer segments (PubMed:27737822). Weakly expressed in rod photoreceptor outer segments (By similarity). May localize to the cilium axoneme (PubMed:27846257). May also be secreted into the interphotoreceptor extracellular matrix (PubMed:27737822).   With evidence from 2 publications.
Centrosome   Localizes to discrete puncta at, or adjacent to, the photoreceptor connecting cilium (PubMed:27737822). Highly expressed in cone photoreceptor outer segments (PubMed:27737822). Weakly expressed in rod photoreceptor outer segments (By similarity). May localize to the cilium axoneme (PubMed:27846257). May also be secreted into the interphotoreceptor extracellular matrix (PubMed:27737822).   With evidence from 2 publications.
Hyaline layer  
Apical lamina  
Spindle   Specifically localized to the apical membrane (PubMed:11076972, PubMed:2344615). Expressed in a mesh punctate pattern that overlaps with metaphase spindle microtubules (PubMed:25065591). In tracheal cells, colocalizes with apn in the subapical region, a small region of the apical membrane apical to the adherens junctions (PubMed:30645584).   With evidence from 7 publications.
Cell junction   Distributed around adherens junction in the apical endfeet through interactions with MAGI1.   With evidence from 12 publications.
Adherens junction   Distributed around adherens junction in the apical endfeet through interactions with MAGI1.   With evidence from 12 publications.
Membrane raft   Distributed around adherens junction in the apical endfeet through interactions with MAGI1.   With evidence from 12 publications.
Endoplasmic reticulum  
Sarcoplasmic reticulum  
Length:
3115
Number of predicted TMHs:
0
Exp number of AAs in TMHs:
0.11214
Exp number, first 60 AAs:
0.00096
Total prob of N-in:
0.00006
outside
1  -  3115
 
 

Population Genetic Test Statistics

Pi
2.779429
Theta
3.50596
Tajima's D
-0.942943
CLR
1.374039
CSRT
0.145992700364982
Interpretation
Uncertain
Peptides ×
Source Sequence Identity Evalue
26280517 GSVIAYISR 95.65 3e-08
26280517 WAEAIR 100.00 0.002
26280517 KPTPFTEEQR 100.00 0.004
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