Gene
KWMTBOMO00323
Pre Gene Modal
BGIBMGA000692
Annotation
PREDICTED:_dynein_heavy_chain_6?_axonemal_[Bombyx_mori]
Full name
Dynein heavy chain 6, axonemal
+ More
Dynein heavy chain 1, axonemal
Dynein heavy chain 7, axonemal
Dynein heavy chain 2, axonemal
Dynein heavy chain 3, axonemal
Dynein-1-beta heavy chain, flagellar inner arm I1 complex
Dynein heavy chain 10, axonemal
Dynein beta chain, ciliary
Dynein heavy chain 9, axonemal
Dynein-1-alpha heavy chain, flagellar inner arm I1 complex
Dynein heavy chain 17, axonemal
Dynein heavy chain 11, axonemal
Dynein beta chain, flagellar outer arm
Dynein heavy chain 8, axonemal
Dynein heavy chain 5, axonemal
Dynein gamma chain, flagellar outer arm
Dynein alpha chain, flagellar outer arm
Dynein heavy chain, cytoplasmic
Dynein heavy chain 12, axonemal
Cytoplasmic dynein 2 heavy chain 1
Cytoplasmic dynein 1 heavy chain 1
Dynein heavy chain-like protein PF11_0240
Dynein heavy chain-like protein MAL7P1.162
Dynein heavy chain domain-containing protein 1
Dynein heavy chain 1, axonemal
Dynein heavy chain 7, axonemal
Dynein heavy chain 2, axonemal
Dynein heavy chain 3, axonemal
Dynein-1-beta heavy chain, flagellar inner arm I1 complex
Dynein heavy chain 10, axonemal
Dynein beta chain, ciliary
Dynein heavy chain 9, axonemal
Dynein-1-alpha heavy chain, flagellar inner arm I1 complex
Dynein heavy chain 17, axonemal
Dynein heavy chain 11, axonemal
Dynein beta chain, flagellar outer arm
Dynein heavy chain 8, axonemal
Dynein heavy chain 5, axonemal
Dynein gamma chain, flagellar outer arm
Dynein alpha chain, flagellar outer arm
Dynein heavy chain, cytoplasmic
Dynein heavy chain 12, axonemal
Cytoplasmic dynein 2 heavy chain 1
Cytoplasmic dynein 1 heavy chain 1
Dynein heavy chain-like protein PF11_0240
Dynein heavy chain-like protein MAL7P1.162
Dynein heavy chain domain-containing protein 1
Alternative Name
Axonemal beta dynein heavy chain 6
Ciliary dynein heavy chain 6
Axonemal beta dynein heavy chain 1
Ciliary dynein heavy chain 1
Heat shock regulated protein 1
hDHC7
mDHC7
Axonemal beta dynein heavy chain 7
Ciliary dynein heavy chain 7
Dynein heavy chain-like protein 2
hDHC2
Axonemal dynein heavy chain b
Dynein-like protein 7
Axonemal beta dynein heavy chain 2
Ciliary dynein heavy chain 2
Axonemal beta dynein heavy chain 3
Ciliary dynein heavy chain 3
Dnahc3-b
Dynein heavy chain domain-containing protein 3
1-beta DHC
Dynein-1, subspecies f
Axonemal beta dynein heavy chain 10
Ciliary dynein heavy chain 10
Axonemal beta dynein heavy chain 9
Ciliary dynein heavy chain 9
1-alpha DHC
Axonemal beta dynein heavy chain 17
Axonemal dynein heavy chain-like protein 1
Ciliary dynein heavy chain 17
Ciliary dynein heavy chain-like protein 1
Dynein light chain 2, axonemal
Axonemal beta dynein heavy chain 11
Ciliary dynein heavy chain 11
Axonemal beta dynein heavy chain 8
Ciliary dynein heavy chain 8
Axonemal beta dynein heavy chain 5
Ciliary dynein heavy chain 5
DHC alpha
Dynein heavy chain, cytosolic
Ropy-1
Bm259
Axonemal beta dynein heavy chain 12
Axonemal dynein heavy chain 12-like protein
Axonemal dynein heavy chain 7-like protein
Ciliary dynein heavy chain 12
Dynein heavy chain 7-like, axonemal
Dynein heavy chain domain-containing protein 2
Cytoplasmic dynein 2 heavy chain
Dynein cytoplasmic heavy chain 2
Dynein heavy chain 11
Dynein heavy chain isotype 1B
Dynein-like protein 4
Abnormal chemotaxis protein 3
Cytoplasmic dynein heavy chain 1
MAP 1C
DHC08
Cytoplasmic dynein heavy chain 1b
Dynein heavy chain domain 1-like protein
Protein CCDC35
Ciliary dynein heavy chain 6
Axonemal beta dynein heavy chain 1
Ciliary dynein heavy chain 1
Heat shock regulated protein 1
hDHC7
mDHC7
Axonemal beta dynein heavy chain 7
Ciliary dynein heavy chain 7
Dynein heavy chain-like protein 2
hDHC2
Axonemal dynein heavy chain b
Dynein-like protein 7
Axonemal beta dynein heavy chain 2
Ciliary dynein heavy chain 2
Axonemal beta dynein heavy chain 3
Ciliary dynein heavy chain 3
Dnahc3-b
Dynein heavy chain domain-containing protein 3
1-beta DHC
Dynein-1, subspecies f
Axonemal beta dynein heavy chain 10
Ciliary dynein heavy chain 10
Axonemal beta dynein heavy chain 9
Ciliary dynein heavy chain 9
1-alpha DHC
Axonemal beta dynein heavy chain 17
Axonemal dynein heavy chain-like protein 1
Ciliary dynein heavy chain 17
Ciliary dynein heavy chain-like protein 1
Dynein light chain 2, axonemal
Axonemal beta dynein heavy chain 11
Ciliary dynein heavy chain 11
Axonemal beta dynein heavy chain 8
Ciliary dynein heavy chain 8
Axonemal beta dynein heavy chain 5
Ciliary dynein heavy chain 5
DHC alpha
Dynein heavy chain, cytosolic
Ropy-1
Bm259
Axonemal beta dynein heavy chain 12
Axonemal dynein heavy chain 12-like protein
Axonemal dynein heavy chain 7-like protein
Ciliary dynein heavy chain 12
Dynein heavy chain 7-like, axonemal
Dynein heavy chain domain-containing protein 2
Cytoplasmic dynein 2 heavy chain
Dynein cytoplasmic heavy chain 2
Dynein heavy chain 11
Dynein heavy chain isotype 1B
Dynein-like protein 4
Abnormal chemotaxis protein 3
Cytoplasmic dynein heavy chain 1
MAP 1C
DHC08
Cytoplasmic dynein heavy chain 1b
Dynein heavy chain domain 1-like protein
Protein CCDC35
Location in the cell
Cytoplasmic Reliability : 2.556
Sequence
CDS
ATGCTAGCGGATATGCTACGTATACACGTTAATTTCACACCGAGTCGCGAGCTATTGGAAGGCTCTGCACTAGATGAAGTTCTTGAAGTACTACCAAGGCAAACTGATACTTGCAAATGGGCTCTGTTCCAAGTGGACGCCTACGTCAGACCGAATGGTGCGGTAGAGCTAAATCCAAGTCAAGAAATTATTTCTTCGTATTTAGAGAAGATTACGAGTTATTGGGATGAGCACGTGCGAAAATTCCGACAATTCTTAACCGAAGAAACATTACAAATGATTGTCCAACCGACGATAATGGGTAAACAGGTCGAGTGGTCTGCTGGCATGTCGCCCAATTTGTATTTTCTAATGAACCAGGACAAGAAGATGTTAGACGACATAACCTTCATTCCAACTTCTATTAAAAATGCATACGAGTGCGTCTGGCTGTTCTTAAACAGAATGCAAGCATTTATGGACAGCTTTAAGGAAGCTCACGAAATGGATGTGAATATTATTAAACAAGAAAGGGATTTGAATGAGTTTAGAAAGCTTTGTGAAAAATTTGTTAAGCAAATGGAAGCTATCGAAGACGTGGTTAGCTACCAACCGTTAGGTTTAATATTTCTATGCTTGAGCCCTTTCCAGGAGCTATTTAGGCCGCAACCCAAGAGATTGTTTGACGTTGTACTCAACGTTACTCCCGATATCGGTCGTGAATGCATTGATGGAATATTGGAAGGAGTTGAGAATATAAGTGGAGATATCACTAAAGATCCTGAAACAGCGAGCGAACTAGTAGCTTTTAATTTCATGTTAGACGGATTAGAATCTCGCGTTGCATTCCTCGAAGAAAGACTGGAATACTTGAGGGAGCTTTACGATCTGATGGGAGAGTTCAATATACCTATTCCACCTGAAGATATGACCCAGTTCTTAGGTCTGAGCGTTACACTCAGTACTCTACGGAGCGATGTCGATGCTAGAATAGAATCGCGTAGCAAACTCGCCGGTATGTTTGCAAGTCAAATTGGCAAAGACATTATGAATTTAATGTTAGATGTTAATAAACTAAGGGATGAAGTTACGCAACCGTGGTTATATGACGAGAAATCGGATCTAGAGAAAGTTATGGAGACACTCGACGATCTATTGGAAAAATTAATGGCATGTTCGGCTCGAGACAAGCAAATCCGGGAATGGCAAAAAATATTCAAGATACCGCCAGCTAGGTTAGAGCAATTAGACGAAGCCATAAATGACGTCAAACTTAGACAGCTTCTTTGGAAAGCATCTAAAGAATGGAACGACATGTTCAAATCTTGGTACGATAATCCTTTTAATACCTTGGACGTAGACGAGATACAAAACACGACAATAAGCTACGGCAAAATATTTAATCAACTGGACAAAGGTTTACCTAGTAATACAATCGTACCGAAATGTAAAGAACTCATCGACGTTATTAAGGAGAAATTACCGGTGATTTCGTATTTACGCAATCCGGCTTTAAAACCACGACACTGGGTGAAAATAGAAGAGATTTTGCACACCCGATTCACGCCTGACGTCGTAATGAATCTGCAAATGTTCGAAGAGCTCCAGGCTTTCCAACATTCTGATGAACTCATGGAAGTTGCCGGTCAAGCTAGTTCGGAAGCTGGTCTCGAGTCTCTATTGAAAAAAGTTGAAGAGATATGGGCCGCTTTGGAGTTTCCCGTTATTTTACATAAAGACGCCAGAGATGTGTATGTCCTCGGTGGCTTAGATGAAATACAAGCGAGTCTTGACGAGAGTAACATTCACATAAGCACAATATTGAGTTCGAGAAACTGTGGTCCGATTAAAAGCCGAGTCGAAGAATGGGCAAAGAATTTGGAGCTTTTCGCTAAGACTTTGGAAGAATGGTATGCATGTCAGCAGACGTGGATGTATTTGGAGGTTATATTCTCGGCGCCTGACATTCAAAGACAGTTGCCAAATGAGACGAGGCTCTTTTCGATTGTCGACAAATCCTGGAAGGATATTATGCGTAAACTTGCTAAGGTTCCATTGGCGATGCCAGCGGCAACGCAACCAAAACTTTACGAGGAGTTCGTACGGAATAATGAAATGTTGGATCAGATAATGAAATGTCTCGAAGCATATTTGGAAACTAAACGTGTGGCTTTCCCTAGATTTTTCTTCTTATCCAATGACGAGCTATTAGAAATTTTAGCACAGACTCGCAATCCGCACGCGGTGCAACCTCACCTCCGAAAATGCTTTGACGCTATAGCCAAATTAGAATTCGGTGTAAAGTTTCCGGAAAGTGAAATGGAGATAGCGGAAGACGGAACTTTAGTCGAAAAGGAAATGTCGTTTCAAACGAGGGACATGCTGCAAGCTAAATTAGCAAAAACTGCGAGCCCTGAAGATTTGACTACAGATATTGTTGCTATGCTATCTCCGGAAGGGGAGAGGGTTAACTTGGGAAAGGGTCTAAAAGCTCGAGGTAATGTTGAAGATTGGTTGGGAAAAGTCGAGGAAGCAATGTTTGCATCAGTGAAACGATGCATGAAATTTGCATTAAAAGAATACATGGTGAATGAACGAGTGGATTGGGTCGAAATGCATCCTAATCAGGTAGTCCTAACCGTCTCACAGATAATGTGGGCCAAAGGAGTCCACGAGGTATTTAATTTGGAGATACCTCTCCGTATCGATACGGGGTTACTGAGCTACGAGAAAAAATGTATATCGGACCTCAATGACTTGGCTGCTTTGACGCGAAAAGATCTGACCTTATTATTTCGAAAGGTTTTGTGTGCTTTGATCACGATCGATGTACATGCAAGGGATACTATATCACATATGGTCGAGAAACACGTTCAAAAAGCAAACGATTTCGAATGGTTAAAAATGATTCGTTATTATTGGGAAGAAGATATCGATAATTGTGTCGCAAGAATGTCTAGTGCCATGTATATATATGGACACGAGTATCTAGGAGCTGGAGGTGTCTTGGTTATAACGCCATTGACGGACCGCTGCTACCTTTGTCTGATGGGAGCTCTCCAGCTTGACCTTGGAGGGGCTCCGGCTGGACCGGCTGGAACCGGAAAGACCGAGACAACTAAAGACTTAGCTAAATCCCTCGCCATACAATGCGTAGTTTTCAATTGTTCTGAAGGCTTAGATTACAAAATGATGGGAAGATTTTTCTCGGGATTAGCTACGTCCGGCGCATGGTGTTGTTTTGATGAATTCAACCGTATTGACATTGAAGTGTTGTCTGTTATCGCTCAGCAACTCATTACGATTCGAAACGCTAAAGTCGCCAAACAAACAAGATTTATGTTTGAGGGACGAGAAATAAAATTAGTGCGCACTTGTGCTGCTTTCATCACAATGAATCCCGGTTACGCGGGAAGAACTGAACTACCCGACAATCTAAAGGCACTTTTCCGGCCAATCTCTATGATGGTACCGGATTACGCACTCATCGCAGAAGTTATTCTGTACTCTGAAGGCTTTGAATCGTCAAAAGGCCTAGCGAAGAAAATGGTTCAAATGTATAAGTTGTCTAGTGAACAACTATCAAAGCAAGACCATTATGATTTCGGAATGAGGGCTGTTAAAAGTGTGCTTGTAATGGCGGGCGCATTAAAAAGAGCTAATCCCGATCAACACGAGGAGATGACGCTTCTCTGCGCCTTGAACGACAGTAACTTGCCTAAGTTCTTAGCTGCAGACGCAATTTTGTTTGCCGGAATTCTGTCTGATTTATTCCCTGGCGTCAGTCTTCCCGCCAGGGATTACGGAGTTATGGAAGATGTCATCAAAATAATTATGTTGGAGCGTAAATTACAAATCGAAATATGTCAAATACGAAAGGTAATACAACTGCACGAGACGATGATAGTGCGTTGGGGCGTTATGTTAGTGGGACCGACCGGTGGAGGGAAAACTGTAGTACTACATGTGCTAGGTGACACGTACACACGGCTTTACGAAAACGGTGTTGAAGGCTCCCAATATCAACCCGTTCGCAAGTACATTATGAATCCGAAAAGTCTAACTATCGGCGAACTCTACGGAGAGGTCAATCTCCAAACACTCGAATGGCATGATGGTATTTTGCCACTGTGTCTCAGAACAGCAGTTCAGTGTTTAAACCCGGATCATCAATGGCTGATCTGCGACGGCCCTGTCGACGCTGTTTGGATTGAAAACATGAACACTGTACTGGACGATAATAAGATGCTTTGTCTCTCTAACTCCGAACGGATCAAATTAACGCCTTATGTGCATATGGTGTTCGAGGTAGCTGATTTAGCTCAAGCATCACCGGCCACCGTCTCACGTTGCGGTATGGTGTATATCGATCCGAACGAAATGGGATATTTGCCGTTCGTACGTTCTTGGCTACAAGAGGGCGTCGAAAAAAATCTATTCAATCAAGAGAATTCCGATTTTATATACGAACTGTTCAAGATGACGCAAGTCGGCTTAGACCACGTTAATTACAATTGTGGTGTTGGAATCAAACAGGTGGACATCAGCAAAGTGAGTGCGCAGTGCTTCCTGCTGGGTGCGCTACTCGCAGAGCCCGGAGATCGATTTGCGGATAAAGCTGCGTTGAAGATTTATATCGCTCATTGCTTCATATTTTGTTATGTGTGGTGTATTGGCGGGAACATTCTAGAAATGAATAGACAATCCTTTGAAGAAGTCATTAAACGACAATTTGAAGAATACGAAGAAGCCGAATATTACCCTCAGGGTTTCAATTTCTTTGACATGTACATGGACACGCGCCAACGTAAATTAAAAGTGTGGGCCGAGATCATTCCAGAATTCATATACGACTGTAATAAGCCGTTTTTCGAGACTTTAGTGCCTACAATCGACACAGTCCGCTACGGATATTTATTCGAGAAACTTCTCGGTGCCGGTAAACCTGTCATGTTTACCGGGAACACTGGTGTAGGTAAAACGTGTATAGCGGTCGAGATTCTAAACAGAATGTCGTTGACGGGATATTATGTGCCGGTCATATTGAATTTCTCGGCTCAAACAAGCAGCCCTCGCACGCAGGAGGTTATTGAGTTACGCTTAGATAAAAGGCCCAGAAAAGCAATCGGAGCTCCGCTTGGTAAGAAGATAATTATATTTATAGACGATGTGAACATGCCCAAATTAGATGTATATGGCGCTCAACCTACAATCGAATTGTTGAGGCAATTTCTCGACTTTGGTGGAGTATACGATCGAGACAAACTGTACTGGAAAGATATATTAGACGTTGTCCTATCTTGTTCATGTGCCCCTCCCGGTGGTGGTAGGAATCCACTGACCGCACGCTTCGTGAGGCATTTCGCAATGCTTTACATAGCTGCGCCTAACGCGGACGCAATGAAAACTATCTTTAAGGCAATCCTCAAAGGGCACATGGAGGATTTTGTACCCGAAGTTTCGGTCCTTGGAGAATCTATCGTCAATGCCGCTGTCGAAGTTTACCTTAAGATTTGCGCTGAATTATTACCAACGCCCGCAAAGTCTCATTACGTATTCAATCTACGTGATTTATCTAAATCTATGCAGGGTGTTTTGCAAGCACAAGCGGCCTATATGAGATCTCCACAAGGAATGCTGAGATTGTTCTATCATGAATGCCTTCGTGTATTTCACGACCGGTTAATAAATATACAGGATAAGAGTTATTTTTATCATCTAATGGCTTCAGTGTGTGAAAAGAACTTCCAAACTCCTATTTTAAGTGTTCCCGATGAACCGATCATTGAACATCCGCCTCTGTTGTTGTTCGGCGATTTTCTCAATTCATCCGTACCCAAAGAGAATAGAACATACCAAGAAATTCCAGACATCTCTAAGCTCATGATTGTATTGAAGGAATATTTGGATGAATACAATTCAACTGCTCGAGCTGAAATGCATTTAGTTCTTTTTCAAGACGCTGTTGAACATGTGGTTAGAGTGGCCAGGGTTTTCAGAGCCGAACGTGGGCATTGTCTCATGGTTGGTCCCGGGGGATCAGGCAGACGCAGTGTGGCTACCCTTGCTGGACATGTCAACGAATGCAAATGTTTGGGCATGGAGTTAAAGAGAAATTATGATACTCCAGAATTTCACGATGACCTTCGAATGATGTATATGAGGGCCGGTGTTAATTGTGAAGATACCGTTTTCTTATTTACGGACACGCAGATAACGAAGGAAGAATTTTTGGAAGATATAAATAATTTGTTGAATTCTGGTGAAGTGCCGAATCTCTTTGAAGGCGATTCATACGAGCAGGTACAGACTGGATGTCGAACTGAAGCAGCGAAAAGTGGAGTCAATCCCTCAGATAGGGACGGCGTCTATTATTTCTTCATTAACCGAGTTAGGGGGAAGCTGCACCTTTGCATCTGCATGAGCCCTGTAGGAGAAGCGTTCAGACGACGGTGCCGGATGTTTCCGTCCTTAGTTAATTGCTGCACGATAGATTGGTTCACGAAATGGCCTCCTGAAGCTTTATTGTCGGTCGCGCACCAATGCCTCCAGCCGCTCGGCAACCAAGAAATAATCACTAAAATATCTAAACTCTGCGTCACTATGCATCAGAATGTGGATATGATGACTGACCGGCTATACATGGAAATGAGGCGGTATTTCTACACTACGCCGAGCAGCTACCTTGATTTGTTGAAGCTGTATTTAGCGCTGCTCGATAAGAAACAACAGCAAATAATTAGAGGACGAGACAGAATTTCATGTGGATTACAGAAATTGTATGAAACATACGACGTTGTTGGAGTGATGGAACAACAGGTTCGCGAAATGGAACCAATACTGGCACGCAAAGCGGCCGAAAGTATCGCTTTGGTAGAAAGACTTAAAATTGAACAGAAAGCTGCTGACGAAGTTAAACAAGCAGTTATGAAAGACGAAGCTGAGGCTAAGATAAAAGCCGAAGAAGTGAAAGAGATTGCAGACGAAGCAAAAGCAGATCTCGCTTTAGCAATGCCAGCTATGGAGGCAGCTCAAAACGCCCTGAAAGCTCTCAATAAAGCAGACATAAATGAATTGAAAGCATTCCAAAAGCCTCCAGCTTTAGTTCGCTTTGTTATGGAGCCTGTTTGTATTTTGATGGGAGTCAAGCCCGACTGGGACTCGACCAAGAAGCTGTTGGCGGATGTGAATTTCATTGGTAAATTAGCAGACTATGATAAAGATCATATTCCTGATGCAACTCTGAAAAAGATTAAAGTGTATCTCACGCACAAAGATTTCAACCCTGATACTGTCGTTAAAGTTTCGAAGGTTTGTCGTTCAATGGTTCTGTGGGTGCAAGCAATAGATATGTACGCTAAAGTTTTCAGAGTTGTGGAACCGAAAATATTAAAACATAAAGAAGCCGCTGCCATTCTTAAAAGTGTTATGGCCGTGCTAAGAGCTAAACAAAAGGAAGTAGAAGCTATTGAAGCACAACTGGCGAAGATGATGGACGAGCTGAAAACGGTGGAAGATGAACGATTAAAGCTCCAAGCAGATGTTGACTTAGCAGCGGCGCGCCTGTCCCGTGCCGGTAAGCTGACTCAAGCTTTAGCCGATGAGAAAACGCGATGGGAAGAGAGCGTTAAGGCGGCTACACAACAACTTCATTGCACGACCGGTGATATCATTGTCGCATCTGGATGCATCGCATACTTTGGCGCGTTCCCGTCGCATTATCGACGCGAGCTGGAACTAAAGTGGATTGCGGAATGCTCGGAGCTGGAAATACCTTCCTCAAATACCTTCGACTTAATATTAGTGATGGCAGACTCGTATACTGTTCGTACTTGGAACTCTCAAGGGCTTCCGCGGGATGCAATATCGACTGAGAACGGTATATTGGTAACTAGGGCGGGTCGTTGGCCTCTTACGATCGACCCTCAGGAACAAGCCAACCGTTGGATTAAAAACATGGAGAGAGATAACGGTCTTCAGATAACTAAACTGAATGACCCGGGATATGTACGTATTCTGGAGAACTGTATACGACTTGGCTGGCCCATGCTTATTGAAGATCTGGGGGAGACGCTCGAGGCCACGTTGTCACCCGTCCTATTGAAACAGACTTTCCTTCAGGCAGGACGACTTCTGATACATCTAGGTGACAGTGACATTGAATACGATACGAATTTCCGTTTGTATATGACAACGAAATTAGCGAATCCCCACTATTTACCGGAGATATGCATACAAGTCACCCTTGTTAACTTTACGGTCACACTATCTGGCCTCGAGGATCAATTGTTAGCGGATGTAGTGCGACTGGAACGACCCGACTTGGAAATTCTTCGCACTGAACTAATCGTGCGCATCAACGCGGACAAGGCGACATTACTAGAAATCGAGGATAAAATCCTCAGACTTTTGTACGCGTCGTCTGGTAATATTTTGGACGACGAAGAACTCATAGAGACACTTAACGAAAGCAAGGAAACCTCTGAAATAATTAATGCTCGTCTCGAAGAAACCGAGGCGACCGAAATAAACATATCCGCAGCGCGAGAGAAGTACCGGACCGTAGCGACAAGGGGCGCGGTACTTTACTTCGCAGTGGCCCAATTAGCGGACATCGATCCTATGTATCAGTTCTCACTCAAGTACTTCAATCAGGTATTCAATGCAGTTATAGAGAAAAGTGAGAAATGCGACTTACTCGAAACCCGCCTTGAAATACTCCATAGAGAGATCACCTTGAACGTATATCGTAATGTTTCGCGAGGGCTCTTCGAAAGACACAAGCTGGTTTTCAGCTTTCTGTTGAACATGGCTGTATACCTGAACGACGGCTTAGTCACAATGGACGAGTGGAATTTCGTACTACGAGGACCGGCAGGAACTAAAGTGGTACCGCCCAAAAAGCCTAATATTGAATCACTTAGCGATCAAATGTGGCTCGCCGTTCATCACTTGGACGAGACCAATGAAAATTTCCGAGGCCTGGTGTCGGACTGTCTGAGGAGAATACCAATAACAATAGGCTCGTTCAATGTGGATATTCACGTGAACAACAACGACAAAACTCCACCGAAAATTAACTGGGATGAAAAGTTGTCCTCGTTTGAGAAATTAATGATTTTAAAATGCTTGAAAGAGGAAAAACTGGTGTTTGCGATCGCTCAATATGTTAGCACTAGCTTGGGTCACATGTTCATCGAAAGTCCAACCGTCCAACTAAATACATTATACGCAGATACTAACTGTGCGATTCCATTGGTCTTTGTCTTGAGCACGGGATCAGATCCATTTGGAGCCTTCCAGAAATTTGCAACCGAGATGGGTATGCGGGACCGTCTTCATTCTATATCATTAGGGCAAGGTCAGGGACCGGTTGCTGAGAAAATGATTAACAATGCTAAACCAAAAGGGGACTGGATATTTTTACAGAATTGTCATTTAGCAGCCTCCTGGATGTTAAGTCTAGAAGTAATCGTGGCCAATTTGGCAAGCGAGCACGGAACCCCACACTCAGACTTCAGACTGTACTTGAGTTCAATGCCTACCGCAAAATTCCCGGTGTCGGTGTTGCAAAACTCTGTTAAGGTCACCAACGAACCACCGAAGGGATTAAAGGCTAACGTCAAAAGGGCCCTTATAGAAATGGAAGAGGACTTCTTTGAAAATCATGTTCTGGGTCAGGATTGGCGAACAATGCTATTCGGTATTTGCATGTTTCATGCTATAATACAGGAACGAAAGAAGTTTGGTCCGCTCGGTTGGAATATTACATACGAATTCAATACAAGCGACCGGGAATGCGCCATGCTCAATCTTCAAATGTTCTGCGCCGACGGACACATACCGTGGGACGCGCTGGAGTATATCACAAGTCAGATAACGTACGGCGGCCGCGTGACCGACATGTGGGACCAACGTTGTTTGACAACCATCTTGAAATTGTTCTTCTCGGCCCCGACGCTCGAGGACGGCTATGTATACTCGCAGTCTGGTAGATATTACTGCCCCAGAGCGGATAAACTAGAAGCATACAAAGAGTACATGGATACTCTGCCCGTGATCGAAGTCCCCGAAGTGTTTGGAATGCACGATAATGCGAATATAGCGTTTGAGAACAAGGAGAGCAATACCCTGATACAGACAATAGTAGAGGTACAGCCGCGCGCGGGCGGCGGGGGCGGCGGCGATACACCTGATCAGATTGTGTGGCGGATCTGTGATCAAGTTCGATCGACCGTTTCGAAAAAGATAGATAAAGCCTCCGTGAACCCTGACCTAATGGTTCCTGACGATATGGGACAGTTACACTCCCTAACTACCGTACTCTTACACGAGACCGACAGATTCAACGCGCTTCTAGCTTTGATTCACTCGTCTCTTGGTGAACTACAAAAAGCTATTAAGGGAATAGTCGTCATGTCGGAAGCATTTGAAGAGGTTTTCAATGCGTTTTTGAATAATCGTGTGCCAGCAATGTGGCACAAGAAGGGCTACAATTCACTGAAGTCTCTCGGTAGCTGGATACACGATCTCGTGCTTCGAATAGATTTTATGGAGAAATGGTTAGTTGACGGTCTACAGCCCAGTAGTTGGGTGTCCGGGTTATTTTTCCCTCAAGGTCTGCTAACGGGCGCATTACAGTCCTACGCGCGAAGATATCGAGTGCCGATAGACGCACTCGTGTACGACTTCAAACCCATACCGTTTTTCTTATCGCAAGACGATGTTTACAAGCACAATAAGAAAAACATAAAGGATGGAGACGATGTGTTTGGAGCGCTGACAGTGCCCGAGGACGGTGTCAATATACACGGTCTATTTATTGATGCAGGCCGATGGGACTCCGAAAATAATTGTCTTGTCGACGCTTTAGCAGGTCAAATGAATCCTCCGCTGCCAGTGGTGTGGTTCTACCCGGTCCTCGAATTGCCAAAACCGGACCCACGTTACCAAGCGCCCCTCTACAAGACGTCAGAGAGAGCAGGCACTTTATCGACTACCGGGCACAGCACTAACTTCGTTCTACCGGTGTTGCTACCGACGCACATGCCACCCGATTTTTGGATCATACGTGGTACCGCCCTACTCACTCAAGTTACAGACTGA
Protein
MLADMLRIHVNFTPSRELLEGSALDEVLEVLPRQTDTCKWALFQVDAYVRPNGAVELNPSQEIISSYLEKITSYWDEHVRKFRQFLTEETLQMIVQPTIMGKQVEWSAGMSPNLYFLMNQDKKMLDDITFIPTSIKNAYECVWLFLNRMQAFMDSFKEAHEMDVNIIKQERDLNEFRKLCEKFVKQMEAIEDVVSYQPLGLIFLCLSPFQELFRPQPKRLFDVVLNVTPDIGRECIDGILEGVENISGDITKDPETASELVAFNFMLDGLESRVAFLEERLEYLRELYDLMGEFNIPIPPEDMTQFLGLSVTLSTLRSDVDARIESRSKLAGMFASQIGKDIMNLMLDVNKLRDEVTQPWLYDEKSDLEKVMETLDDLLEKLMACSARDKQIREWQKIFKIPPARLEQLDEAINDVKLRQLLWKASKEWNDMFKSWYDNPFNTLDVDEIQNTTISYGKIFNQLDKGLPSNTIVPKCKELIDVIKEKLPVISYLRNPALKPRHWVKIEEILHTRFTPDVVMNLQMFEELQAFQHSDELMEVAGQASSEAGLESLLKKVEEIWAALEFPVILHKDARDVYVLGGLDEIQASLDESNIHISTILSSRNCGPIKSRVEEWAKNLELFAKTLEEWYACQQTWMYLEVIFSAPDIQRQLPNETRLFSIVDKSWKDIMRKLAKVPLAMPAATQPKLYEEFVRNNEMLDQIMKCLEAYLETKRVAFPRFFFLSNDELLEILAQTRNPHAVQPHLRKCFDAIAKLEFGVKFPESEMEIAEDGTLVEKEMSFQTRDMLQAKLAKTASPEDLTTDIVAMLSPEGERVNLGKGLKARGNVEDWLGKVEEAMFASVKRCMKFALKEYMVNERVDWVEMHPNQVVLTVSQIMWAKGVHEVFNLEIPLRIDTGLLSYEKKCISDLNDLAALTRKDLTLLFRKVLCALITIDVHARDTISHMVEKHVQKANDFEWLKMIRYYWEEDIDNCVARMSSAMYIYGHEYLGAGGVLVITPLTDRCYLCLMGALQLDLGGAPAGPAGTGKTETTKDLAKSLAIQCVVFNCSEGLDYKMMGRFFSGLATSGAWCCFDEFNRIDIEVLSVIAQQLITIRNAKVAKQTRFMFEGREIKLVRTCAAFITMNPGYAGRTELPDNLKALFRPISMMVPDYALIAEVILYSEGFESSKGLAKKMVQMYKLSSEQLSKQDHYDFGMRAVKSVLVMAGALKRANPDQHEEMTLLCALNDSNLPKFLAADAILFAGILSDLFPGVSLPARDYGVMEDVIKIIMLERKLQIEICQIRKVIQLHETMIVRWGVMLVGPTGGGKTVVLHVLGDTYTRLYENGVEGSQYQPVRKYIMNPKSLTIGELYGEVNLQTLEWHDGILPLCLRTAVQCLNPDHQWLICDGPVDAVWIENMNTVLDDNKMLCLSNSERIKLTPYVHMVFEVADLAQASPATVSRCGMVYIDPNEMGYLPFVRSWLQEGVEKNLFNQENSDFIYELFKMTQVGLDHVNYNCGVGIKQVDISKVSAQCFLLGALLAEPGDRFADKAALKIYIAHCFIFCYVWCIGGNILEMNRQSFEEVIKRQFEEYEEAEYYPQGFNFFDMYMDTRQRKLKVWAEIIPEFIYDCNKPFFETLVPTIDTVRYGYLFEKLLGAGKPVMFTGNTGVGKTCIAVEILNRMSLTGYYVPVILNFSAQTSSPRTQEVIELRLDKRPRKAIGAPLGKKIIIFIDDVNMPKLDVYGAQPTIELLRQFLDFGGVYDRDKLYWKDILDVVLSCSCAPPGGGRNPLTARFVRHFAMLYIAAPNADAMKTIFKAILKGHMEDFVPEVSVLGESIVNAAVEVYLKICAELLPTPAKSHYVFNLRDLSKSMQGVLQAQAAYMRSPQGMLRLFYHECLRVFHDRLINIQDKSYFYHLMASVCEKNFQTPILSVPDEPIIEHPPLLLFGDFLNSSVPKENRTYQEIPDISKLMIVLKEYLDEYNSTARAEMHLVLFQDAVEHVVRVARVFRAERGHCLMVGPGGSGRRSVATLAGHVNECKCLGMELKRNYDTPEFHDDLRMMYMRAGVNCEDTVFLFTDTQITKEEFLEDINNLLNSGEVPNLFEGDSYEQVQTGCRTEAAKSGVNPSDRDGVYYFFINRVRGKLHLCICMSPVGEAFRRRCRMFPSLVNCCTIDWFTKWPPEALLSVAHQCLQPLGNQEIITKISKLCVTMHQNVDMMTDRLYMEMRRYFYTTPSSYLDLLKLYLALLDKKQQQIIRGRDRISCGLQKLYETYDVVGVMEQQVREMEPILARKAAESIALVERLKIEQKAADEVKQAVMKDEAEAKIKAEEVKEIADEAKADLALAMPAMEAAQNALKALNKADINELKAFQKPPALVRFVMEPVCILMGVKPDWDSTKKLLADVNFIGKLADYDKDHIPDATLKKIKVYLTHKDFNPDTVVKVSKVCRSMVLWVQAIDMYAKVFRVVEPKILKHKEAAAILKSVMAVLRAKQKEVEAIEAQLAKMMDELKTVEDERLKLQADVDLAAARLSRAGKLTQALADEKTRWEESVKAATQQLHCTTGDIIVASGCIAYFGAFPSHYRRELELKWIAECSELEIPSSNTFDLILVMADSYTVRTWNSQGLPRDAISTENGILVTRAGRWPLTIDPQEQANRWIKNMERDNGLQITKLNDPGYVRILENCIRLGWPMLIEDLGETLEATLSPVLLKQTFLQAGRLLIHLGDSDIEYDTNFRLYMTTKLANPHYLPEICIQVTLVNFTVTLSGLEDQLLADVVRLERPDLEILRTELIVRINADKATLLEIEDKILRLLYASSGNILDDEELIETLNESKETSEIINARLEETEATEINISAAREKYRTVATRGAVLYFAVAQLADIDPMYQFSLKYFNQVFNAVIEKSEKCDLLETRLEILHREITLNVYRNVSRGLFERHKLVFSFLLNMAVYLNDGLVTMDEWNFVLRGPAGTKVVPPKKPNIESLSDQMWLAVHHLDETNENFRGLVSDCLRRIPITIGSFNVDIHVNNNDKTPPKINWDEKLSSFEKLMILKCLKEEKLVFAIAQYVSTSLGHMFIESPTVQLNTLYADTNCAIPLVFVLSTGSDPFGAFQKFATEMGMRDRLHSISLGQGQGPVAEKMINNAKPKGDWIFLQNCHLAASWMLSLEVIVANLASEHGTPHSDFRLYLSSMPTAKFPVSVLQNSVKVTNEPPKGLKANVKRALIEMEEDFFENHVLGQDWRTMLFGICMFHAIIQERKKFGPLGWNITYEFNTSDRECAMLNLQMFCADGHIPWDALEYITSQITYGGRVTDMWDQRCLTTILKLFFSAPTLEDGYVYSQSGRYYCPRADKLEAYKEYMDTLPVIEVPEVFGMHDNANIAFENKESNTLIQTIVEVQPRAGGGGGGDTPDQIVWRICDQVRSTVSKKIDKASVNPDLMVPDDMGQLHSLTTVLLHETDRFNALLALIHSSLGELQKAIKGIVVMSEAFEEVFNAFLNNRVPAMWHKKGYNSLKSLGSWIHDLVLRIDFMEKWLVDGLQPSSWVSGLFFPQGLLTGALQSYARRYRVPIDALVYDFKPIPFFLSQDDVYKHNKKNIKDGDDVFGALTVPEDGVNIHGLFIDAGRWDSENNCLVDALAGQMNPPLPVVWFYPVLELPKPDPRYQAPLYKTSERAGTLSTTGHSTNFVLPVLLPTHMPPDFWIIRGTALLTQVTD
Summary
Description
Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP (By similarity).
Force generating protein of cilia required for sperm flagellum motility. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required in spermatozoa for the formation of the inner dynein arms and biogenesis of the axoneme (PubMed:24360805).
Force generating protein of cilia required for sperm flagellum motility (PubMed:11371505). Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP (By similarity). Required in spermatozoa for the formation of the inner dynein arms and biogenesis of the axoneme (By similarity).
Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Involved in sperm motility; implicated in sperm flagellar assembly (By similarity).
Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Involved in sperm motility; implicated in sperm flagellar assembly (By similarity). Probable inner arm dynein heavy chain.
Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Involved in sperm motility; implicated in sperm flagellar assembly.
Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required for structural and functional integrity of the cilia of ependymal cells lining the brain ventricles.
Force generating protein of cilia required for sperm flagellum motility. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required in spermatozoa for the formation of the inner dynein arms and biogenesis of the axoneme (By similarity).
May function as a motor for intraflagellar retrograde transport. Functions in cilia biogenesis. May play a role in transport between endoplasmic reticulum and Golgi or organization of the Golgi in cells (By similarity).
May function as a motor for intraflagellar retrograde transport. Functions in cilia biogenesis. According to PubMed:8666668, it may play a role in transport between endoplasmic reticulum and Golgi or organization of the Golgi in cells.
May function as a motor for intraflagellar retrograde transport. Functions in cilia biogenesis (By similarity).
Functions as a motor for intraflagellar retrograde transport in chemosensory neurons (PubMed:10545497, PubMed:28479320). Functions in cilia biogenesis (PubMed:10545497, PubMed:27515926).
Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Plays a role in mitotic spindle assembly and metaphase plate congression (PubMed:27462074).
Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Plays a role in mitotic spindle assembly and metaphase plate congression.
Cytoplasmic dynein acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required to maintain uniform nuclear distribution in hyphae. May play an important role in the proper orientation of the mitotic spindle into the budding daughter cell yeast. Probably required for normal progression of the cell cycle.
Cytoplasmic dynein acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules (By similarity). Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP (By similarity). May play a role in nuclear migration in hypodermal precursor cells (PubMed:20005871, PubMed:27697906). May be involved in the transport of synaptic vesicle components towards the axon of the DA motor neuron (PubMed:20510931). This function may involve the regulation of dynein by pct-1 and/or cdk-5 (PubMed:20510931). Involved in the formation of synapses in the dorsal region during synaptic remodeling of DD motor neurons (PubMed:21609829). Required for anterograde trafficking of dense-core vesicles in the DB motor neuron dendrites (PubMed:22699897). Required for the formation of dendritic branches of PVD sensory neurons (PubMed:21205795). May also play a role in GABAergic synaptic vesicle localization in the ventral nerve cord (PubMed:16996038). May play a role in the pairing of homologous chromosomes during meiosis (PubMed:26483555).
May function as a motor for intraflagellar retrograde transport. Functions in flagellar biogenesis.
Acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP (By similarity).
Cytoplasmic dynein acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required for nuclear movement during meiotic prophase.
Force generating protein of cilia required for sperm flagellum motility. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required in spermatozoa for the formation of the inner dynein arms and biogenesis of the axoneme (PubMed:24360805).
Force generating protein of cilia required for sperm flagellum motility (PubMed:11371505). Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP (By similarity). Required in spermatozoa for the formation of the inner dynein arms and biogenesis of the axoneme (By similarity).
Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Involved in sperm motility; implicated in sperm flagellar assembly (By similarity).
Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Involved in sperm motility; implicated in sperm flagellar assembly (By similarity). Probable inner arm dynein heavy chain.
Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Involved in sperm motility; implicated in sperm flagellar assembly.
Force generating protein of respiratory cilia. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required for structural and functional integrity of the cilia of ependymal cells lining the brain ventricles.
Force generating protein of cilia required for sperm flagellum motility. Produces force towards the minus ends of microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required in spermatozoa for the formation of the inner dynein arms and biogenesis of the axoneme (By similarity).
May function as a motor for intraflagellar retrograde transport. Functions in cilia biogenesis. May play a role in transport between endoplasmic reticulum and Golgi or organization of the Golgi in cells (By similarity).
May function as a motor for intraflagellar retrograde transport. Functions in cilia biogenesis. According to PubMed:8666668, it may play a role in transport between endoplasmic reticulum and Golgi or organization of the Golgi in cells.
May function as a motor for intraflagellar retrograde transport. Functions in cilia biogenesis (By similarity).
Functions as a motor for intraflagellar retrograde transport in chemosensory neurons (PubMed:10545497, PubMed:28479320). Functions in cilia biogenesis (PubMed:10545497, PubMed:27515926).
Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Plays a role in mitotic spindle assembly and metaphase plate congression (PubMed:27462074).
Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Plays a role in mitotic spindle assembly and metaphase plate congression.
Cytoplasmic dynein acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required to maintain uniform nuclear distribution in hyphae. May play an important role in the proper orientation of the mitotic spindle into the budding daughter cell yeast. Probably required for normal progression of the cell cycle.
Cytoplasmic dynein acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules (By similarity). Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP (By similarity). May play a role in nuclear migration in hypodermal precursor cells (PubMed:20005871, PubMed:27697906). May be involved in the transport of synaptic vesicle components towards the axon of the DA motor neuron (PubMed:20510931). This function may involve the regulation of dynein by pct-1 and/or cdk-5 (PubMed:20510931). Involved in the formation of synapses in the dorsal region during synaptic remodeling of DD motor neurons (PubMed:21609829). Required for anterograde trafficking of dense-core vesicles in the DB motor neuron dendrites (PubMed:22699897). Required for the formation of dendritic branches of PVD sensory neurons (PubMed:21205795). May also play a role in GABAergic synaptic vesicle localization in the ventral nerve cord (PubMed:16996038). May play a role in the pairing of homologous chromosomes during meiosis (PubMed:26483555).
May function as a motor for intraflagellar retrograde transport. Functions in flagellar biogenesis.
Acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP (By similarity).
Cytoplasmic dynein acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. Required for nuclear movement during meiotic prophase.
Subunit
The dynein complex consists of at least two heavy chains and a number of intermediate and light chains.
Consists of at least two heavy chains and a number of intermediate and light chains.
The I1 inner arm complex (also known as the f dynein complex) is a two-headed isoform composed of two heavy chains (1-alpha and 1-beta), three intermediate chains and three light chains. I1 occupies a specific position proximal to the first radial spoke and repeats every 96 nm along the length of the axoneme.
Consists of at least two heavy chains (alpha and beta), three intermediate chains and several light chains.
Consists of at least 3 heavy chains (alpha, beta and gamma), 2 intermediate chains and 8 light chains.
Interacts with DNAL1 (By similarity). Consists of at least two heavy chains and a number of intermediate and light chains.
Interacts with DNAL1 (PubMed:21496787). Consists of at least two heavy chains and a number of intermediate and light chains.
The cytoplasmic dynein complex 2 is probably composed by a heavy chain DYNC2H1 homodimer and a number of DYNC2LI1 light intermediate chains.
The cytoplasmic dynein complex 2 is probably composed by a heavy chain DYH1B homodimer and a number of light intermediate chains.
The cytoplasmic dynein complex 2 is probably composed by a heavy chain che-3 homodimer and a number of light intermediate chains.
Homodimer. The cytoplasmic dynein 1 complex consists of two catalytic heavy chains (HCs) and a number of non-catalytic subunits presented by intermediate chains (ICs), light intermediate chains (LICs) and light chains (LCs); the composition seems to vary in respect to the IC, LIC and LC composition. The heavy chain homodimer serves as a scaffold for the probable homodimeric assembly of the respective non-catalytic subunits. The ICs and LICs bind directly to the HC dimer and dynein LCs assemble on the IC dimer. Interacts with DYNC1LI1; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1LI2; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1I2 (By similarity). Interacts with BICD2 (PubMed:25512093).
Homodimer. The cytoplasmic dynein 1 complex consists of two catalytic heavy chains (HCs) and a number of non-catalytic subunits presented by intermediate chains (ICs), light intermediate chains (LICs) and light chains (LCs); the composition seems to vary in respect to the IC, LIC and LC composition. The heavy chain homodimer serves as a scaffold for the probable homodimeric assembly of the respective non-catalytic subunits. The ICs and LICs bind directly to the HC dimer and dynein LCs assemble on the IC dimer (PubMed:2140361). Interacts with DYNC1LI1; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1LI2; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1I2 (PubMed:10893223). Interacts with BICD2 (By similarity).
Homodimer. The cytoplasmic dynein 1 complex consists of two catalytic heavy chains (HCs) and a number of non-catalytic subunits presented by intermediate chains (ICs), light intermediate chains (LICs) and light chains (LCs); the composition seems to vary in respect to the IC, LIC and LC composition. The heavy chain homodimer serves as a scaffold for the probable homodimeric assembly of the respective non-catalytic subunits. The ICs and LICs bind directly to the HC dimer and dynein LCs assemble on the IC dimer. Interacts with DYNC1LI1; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1LI2; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1I2 (By similarity). Interacts with BICD2 (PubMed:22956769).
The dynein complex consists of at least two heavy chains and a number of intermediate and light chains. Interacts with DYN3.
The cytoplasmic dynein complex 2 is probably composed by a DHC1B homodimer and a number of D1BLIC light intermediate chains. Interacts with FAP133, FLA10 and LC8.
Consists of at least two heavy chains and a number of intermediate and light chains.
The I1 inner arm complex (also known as the f dynein complex) is a two-headed isoform composed of two heavy chains (1-alpha and 1-beta), three intermediate chains and three light chains. I1 occupies a specific position proximal to the first radial spoke and repeats every 96 nm along the length of the axoneme.
Consists of at least two heavy chains (alpha and beta), three intermediate chains and several light chains.
Consists of at least 3 heavy chains (alpha, beta and gamma), 2 intermediate chains and 8 light chains.
Interacts with DNAL1 (By similarity). Consists of at least two heavy chains and a number of intermediate and light chains.
Interacts with DNAL1 (PubMed:21496787). Consists of at least two heavy chains and a number of intermediate and light chains.
The cytoplasmic dynein complex 2 is probably composed by a heavy chain DYNC2H1 homodimer and a number of DYNC2LI1 light intermediate chains.
The cytoplasmic dynein complex 2 is probably composed by a heavy chain DYH1B homodimer and a number of light intermediate chains.
The cytoplasmic dynein complex 2 is probably composed by a heavy chain che-3 homodimer and a number of light intermediate chains.
Homodimer. The cytoplasmic dynein 1 complex consists of two catalytic heavy chains (HCs) and a number of non-catalytic subunits presented by intermediate chains (ICs), light intermediate chains (LICs) and light chains (LCs); the composition seems to vary in respect to the IC, LIC and LC composition. The heavy chain homodimer serves as a scaffold for the probable homodimeric assembly of the respective non-catalytic subunits. The ICs and LICs bind directly to the HC dimer and dynein LCs assemble on the IC dimer. Interacts with DYNC1LI1; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1LI2; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1I2 (By similarity). Interacts with BICD2 (PubMed:25512093).
Homodimer. The cytoplasmic dynein 1 complex consists of two catalytic heavy chains (HCs) and a number of non-catalytic subunits presented by intermediate chains (ICs), light intermediate chains (LICs) and light chains (LCs); the composition seems to vary in respect to the IC, LIC and LC composition. The heavy chain homodimer serves as a scaffold for the probable homodimeric assembly of the respective non-catalytic subunits. The ICs and LICs bind directly to the HC dimer and dynein LCs assemble on the IC dimer (PubMed:2140361). Interacts with DYNC1LI1; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1LI2; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1I2 (PubMed:10893223). Interacts with BICD2 (By similarity).
Homodimer. The cytoplasmic dynein 1 complex consists of two catalytic heavy chains (HCs) and a number of non-catalytic subunits presented by intermediate chains (ICs), light intermediate chains (LICs) and light chains (LCs); the composition seems to vary in respect to the IC, LIC and LC composition. The heavy chain homodimer serves as a scaffold for the probable homodimeric assembly of the respective non-catalytic subunits. The ICs and LICs bind directly to the HC dimer and dynein LCs assemble on the IC dimer. Interacts with DYNC1LI1; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1LI2; DYNC1LI1 and DYNC1LI2 bind mutually exclusive to DYNC1H1. Interacts with DYNC1I2 (By similarity). Interacts with BICD2 (PubMed:22956769).
The dynein complex consists of at least two heavy chains and a number of intermediate and light chains. Interacts with DYN3.
The cytoplasmic dynein complex 2 is probably composed by a DHC1B homodimer and a number of D1BLIC light intermediate chains. Interacts with FAP133, FLA10 and LC8.
Miscellaneous
Mice homozygous for Dync2h1 null alleles die at approximately 12.5 dpc with abnormal brain morphology, frequent heart-looping and occasionally with polysyndactily. Cilia have abnormal morphology.
Present with 195 molecules/cell in log phase SD medium.
Present with 195 molecules/cell in log phase SD medium.
Similarity
Belongs to the dynein heavy chain family.
Keywords
Alternative splicing
ATP-binding
Cell projection
Cilium
Coiled coil
Complete proteome
Cytoplasm
Cytoskeleton
Dynein
Microtubule
Motor protein
Nucleotide-binding
Polymorphism
Reference proteome
Repeat
Ciliopathy
Disease mutation
Flagellum
Kartagener syndrome
Primary ciliary dyskinesia
TPR repeat
RNA editing
Glycoprotein
3D-structure
Direct protein sequencing
Kelch repeat
Phosphoprotein
Ubl conjugation pathway
Cell membrane
Developmental protein
Membrane
Karyogamy
Acetylation
Cell cycle
Cell division
Charcot-Marie-Tooth disease
Mental retardation
Mitosis
Neurodegeneration
Neuropathy
Transport
Neurogenesis
Merozoite
Feature
chain Dynein heavy chain 6, axonemal
splice variant In isoform 2.
sequence variant Found in a patient with azoospermia; unknown pathological significance; dbSNP:rs61731722.
splice variant In isoform 2.
sequence variant Found in a patient with azoospermia; unknown pathological significance; dbSNP:rs61731722.
Uniprot
Q9C0G6.3
Q9P2D7.5
E9Q8T7.1
Q8WXX0.2
Q63170.2
P0C6F1.1
+ More
Q8TD57.1 Q9P225.3 Q8BW94.2 Q9MBF8.1 Q8IVF4.4 P23098.1 P39057.1 Q9NYC9.3 Q9SMH3.1 Q9UFH2.3 Q96DT5.4 Q69Z23.2 Q39565.1 Q96JB1.2 Q91XQ0.2 Q8VHE6.2 Q8TE73.3 Q39575.1 Q63164.2 Q39610.2 P45444.2 P45443.1 P78716.1 Q923J6.2 Q3V0Q1.2 Q6ZR08.2 Q8NCM8.4 Q45VK7.1 Q9JJ79.1 Q27802.2 M0R8U1.1 Q19542.2 Q9C1M7.1 P37276.2 Q14204.5 P38650.1 Q9JHU4.2 P36022.1 Q27171.1 Q19020.1 Q9SMH5.2 Q8IID4.1 O13290.1 Q8IBG1.2 Q96M86.2
Q8TD57.1 Q9P225.3 Q8BW94.2 Q9MBF8.1 Q8IVF4.4 P23098.1 P39057.1 Q9NYC9.3 Q9SMH3.1 Q9UFH2.3 Q96DT5.4 Q69Z23.2 Q39565.1 Q96JB1.2 Q91XQ0.2 Q8VHE6.2 Q8TE73.3 Q39575.1 Q63164.2 Q39610.2 P45444.2 P45443.1 P78716.1 Q923J6.2 Q3V0Q1.2 Q6ZR08.2 Q8NCM8.4 Q45VK7.1 Q9JJ79.1 Q27802.2 M0R8U1.1 Q19542.2 Q9C1M7.1 P37276.2 Q14204.5 P38650.1 Q9JHU4.2 P36022.1 Q27171.1 Q19020.1 Q9SMH5.2 Q8IID4.1 O13290.1 Q8IBG1.2 Q96M86.2
Pubmed
14702039
17974005
15815621
15489334
8812413
11175280
+ More
11214970 28206990 10718198 16641997 9373155 9256245 24360805 25927852 27798045 28552195 29449551 16141072 19468303 11371505 19131326 21183079 11877439 10231032 15057822 7657712 8741840 10493829 16959974 10819331 16625196 20835228 10888669 10069812 2957507 2137128 9008712 16541075 19159218 1830927 1833761 11250194 1830928 11247663 9205841 11104725 10459015 8889521 9247642 9545504 18669648 12142464 12853948 18022865 25186273 15368895 8006077 12297094 14574404 18691976 10602986 16054618 11912187 11788826 15269178 11062149 10997877 21496787 16627867 7516341 9186009 8134356 16372000 19146970 7929559 12712197 11489260 8666668 16554811 8186465 12056414 16440056 21211617 21269460 19361615 19442771 22499340 23456818 16061793 12432068 11907264 16229832 8832411 9450951 9851916 10545497 27515926 28479320 11181180 15001715 23749448 8089180 10731132 12537572 8186464 12537569 8227145 14654843 17081983 19690332 19608861 20068231 22223895 23186163 24275569 25944712 27462074 21076407 21820100 22368300 22847149 22459677 23033978 23603762 25512093 24307404 25484024 26846447 28193117 7690137 7684232 2140361 10893223 12730604 18034455 22956769 23806337 8248224 8196765 24374639 8234262 14562095 14562106 15642746 8589455 8056840 8674131 16996038 20510931 20005871 20599902 21205795 21609829 22699897 26483555 27697906 27864381 12802074 17932292 9971742 15269286 17895364 12368864 17653272 10366596 11859360 12368867 12693554 12975309
11214970 28206990 10718198 16641997 9373155 9256245 24360805 25927852 27798045 28552195 29449551 16141072 19468303 11371505 19131326 21183079 11877439 10231032 15057822 7657712 8741840 10493829 16959974 10819331 16625196 20835228 10888669 10069812 2957507 2137128 9008712 16541075 19159218 1830927 1833761 11250194 1830928 11247663 9205841 11104725 10459015 8889521 9247642 9545504 18669648 12142464 12853948 18022865 25186273 15368895 8006077 12297094 14574404 18691976 10602986 16054618 11912187 11788826 15269178 11062149 10997877 21496787 16627867 7516341 9186009 8134356 16372000 19146970 7929559 12712197 11489260 8666668 16554811 8186465 12056414 16440056 21211617 21269460 19361615 19442771 22499340 23456818 16061793 12432068 11907264 16229832 8832411 9450951 9851916 10545497 27515926 28479320 11181180 15001715 23749448 8089180 10731132 12537572 8186464 12537569 8227145 14654843 17081983 19690332 19608861 20068231 22223895 23186163 24275569 25944712 27462074 21076407 21820100 22368300 22847149 22459677 23033978 23603762 25512093 24307404 25484024 26846447 28193117 7690137 7684232 2140361 10893223 12730604 18034455 22956769 23806337 8248224 8196765 24374639 8234262 14562095 14562106 15642746 8589455 8056840 8674131 16996038 20510931 20005871 20599902 21205795 21609829 22699897 26483555 27697906 27864381 12802074 17932292 9971742 15269286 17895364 12368864 17653272 10366596 11859360 12368867 12693554 12975309
EMBL
AK027182
AK094676
AL512706
AC010087
AC096770
AC098975
+ More
AC109827 CH471053 BC015442 BC104884 BC113424 BC117259 BC143666 U61736 AJ132086 AB051484 AB037831 AK023766 AK074130 AK125990 AB290163 AC092045 KF459588 AJ132083 AJ132094 U61738 Z83804 U83571 AY221994 AL117428 AK053204 AC108416 CH466573 BC023155 Z83815 AF327442 AB023161 AK094515 CR749651 AC013274 AC068919 AC104600 AC114760 BC029567 AJ132084 AJ132093 Z83801 AABR03068169 AABR03068266 AABR03068762 AABR03068958 AABR03068975 AABR03069173 AABR03069339 AABR03069471 AABR03070154 AABR03071231 AABR03071501 AABR03071646 AABR03071706 AABR03071857 AABR03072256 D26498 U32180 AL596125 AL731687 Z83813 AK029791 AF494040 AK056509 CH471228 AJ132085 AJ132092 Z83805 U83574 BC019878 AL096732 AC002394 AB040936 AK128517 AK292607 AC025335 AC087388 BC034225 U83570 AC122853 AC131702 Z83816 BC051401 AK053178 AJ242523 AJ242524 AJ242525 AJ132799 AC079315 AC117503 AK095581 AK125475 AK125796 AB095937 AJ132089 X59603 D01021 AF257737 AJ404468 AC005209 AC005410 AC005701 BC128421 AB002355 AJ132088 AJ243806 U61364 AC016182 AC061992 KF510431 AK097776 BC105107 Z83799 AL122077 AJ000522 AJ320497 AC004595 AC102952 AC073102 AC013481 AC005078 AC004002 AC099653 AJ132087 AL591204 AL591433 Z83807 AK173343 U02963 AF356519 AL034345 AL035555 AL035690 AL353700 AL391415 Z83806 AJ132091 AF356520 AF356521 AF356522 AF356523 AF363577 AF342999 AC165951 AC165962 AC166166 AC174471 AF117305 Z83817 AK133238 AF466704 AC131997 AC154880 AK052643 AY045575 AY049075 U61735 AB046823 AK026756 U15303 AABR03100255 AABR03101829 AABR03101330 D26492 L26049 U03904 AACD01000004 BN001308 L31504 CM002239 U84215 AABR03100937 AABR03102926 AABR03102110 AABR03100400 AABR03102032 AABR03101661 AABR03100963 AY032856 AC121919 AC133179 AK076605 AK132980 AK097746 AK126276 AK128592 AC092418 AC093928 AC121250 U53532 AB231765 AB231766 AP000817 AP001486 AP002829 AP002961 AP003382 AP003461 AK021818 AK095579 AK125524 AK131453 U53531 U20552 Z83800 BX538093 AB082528 DQ104402 AK014500 AK032860 AK045978 AK046538 AK083433 AK084796 AC155908 CT010499 AY452064 AY452065 AY452066 AY452067 Z83809 AK173324 AB041881 U61748 D26495 U03969 AABR07008948 Z75536 AF287477 AE016816 L23195 AE014296 L25122 AY051501 AB002323 AB290157 AY682080 U53530 L23958 BC021297 D13896 L08505 AY004877 AC152827 Z21877 L15626 Z28279 BK006944 U20449 L17132 L33260 BX284601 AJ132478 DS496110 AF096277 AE014186 AAN35824.1 AB006784 CU329670 AL844506 AK057314 AK093028 BC111765 BC117301 BC117303 AC009796 AC084337 CH471064 AK074178 AL137619 AY358770
AC109827 CH471053 BC015442 BC104884 BC113424 BC117259 BC143666 U61736 AJ132086 AB051484 AB037831 AK023766 AK074130 AK125990 AB290163 AC092045 KF459588 AJ132083 AJ132094 U61738 Z83804 U83571 AY221994 AL117428 AK053204 AC108416 CH466573 BC023155 Z83815 AF327442 AB023161 AK094515 CR749651 AC013274 AC068919 AC104600 AC114760 BC029567 AJ132084 AJ132093 Z83801 AABR03068169 AABR03068266 AABR03068762 AABR03068958 AABR03068975 AABR03069173 AABR03069339 AABR03069471 AABR03070154 AABR03071231 AABR03071501 AABR03071646 AABR03071706 AABR03071857 AABR03072256 D26498 U32180 AL596125 AL731687 Z83813 AK029791 AF494040 AK056509 CH471228 AJ132085 AJ132092 Z83805 U83574 BC019878 AL096732 AC002394 AB040936 AK128517 AK292607 AC025335 AC087388 BC034225 U83570 AC122853 AC131702 Z83816 BC051401 AK053178 AJ242523 AJ242524 AJ242525 AJ132799 AC079315 AC117503 AK095581 AK125475 AK125796 AB095937 AJ132089 X59603 D01021 AF257737 AJ404468 AC005209 AC005410 AC005701 BC128421 AB002355 AJ132088 AJ243806 U61364 AC016182 AC061992 KF510431 AK097776 BC105107 Z83799 AL122077 AJ000522 AJ320497 AC004595 AC102952 AC073102 AC013481 AC005078 AC004002 AC099653 AJ132087 AL591204 AL591433 Z83807 AK173343 U02963 AF356519 AL034345 AL035555 AL035690 AL353700 AL391415 Z83806 AJ132091 AF356520 AF356521 AF356522 AF356523 AF363577 AF342999 AC165951 AC165962 AC166166 AC174471 AF117305 Z83817 AK133238 AF466704 AC131997 AC154880 AK052643 AY045575 AY049075 U61735 AB046823 AK026756 U15303 AABR03100255 AABR03101829 AABR03101330 D26492 L26049 U03904 AACD01000004 BN001308 L31504 CM002239 U84215 AABR03100937 AABR03102926 AABR03102110 AABR03100400 AABR03102032 AABR03101661 AABR03100963 AY032856 AC121919 AC133179 AK076605 AK132980 AK097746 AK126276 AK128592 AC092418 AC093928 AC121250 U53532 AB231765 AB231766 AP000817 AP001486 AP002829 AP002961 AP003382 AP003461 AK021818 AK095579 AK125524 AK131453 U53531 U20552 Z83800 BX538093 AB082528 DQ104402 AK014500 AK032860 AK045978 AK046538 AK083433 AK084796 AC155908 CT010499 AY452064 AY452065 AY452066 AY452067 Z83809 AK173324 AB041881 U61748 D26495 U03969 AABR07008948 Z75536 AF287477 AE016816 L23195 AE014296 L25122 AY051501 AB002323 AB290157 AY682080 U53530 L23958 BC021297 D13896 L08505 AY004877 AC152827 Z21877 L15626 Z28279 BK006944 U20449 L17132 L33260 BX284601 AJ132478 DS496110 AF096277 AE014186 AAN35824.1 AB006784 CU329670 AL844506 AK057314 AK093028 BC111765 BC117301 BC117303 AC009796 AC084337 CH471064 AK074178 AL137619 AY358770
Proteomes
PRIDE
Q9C0G6
Q9P2D7
E9Q8T7
Q8WXX0
Q63170
P0C6F1
+ More
Q8TD57 Q9P225 Q8BW94 Q9MBF8 Q8IVF4 P23098 P39057 Q9NYC9 Q9SMH3 Q9UFH2 Q96DT5 Q69Z23 Q39565 Q96JB1 Q91XQ0 Q8VHE6 Q8TE73 Q39575 Q63164 Q39610 P45444 P45443 P78716 Q923J6 Q3V0Q1 Q6ZR08 Q8NCM8 Q45VK7 Q9JJ79 Q27802 M0R8U1 Q19542 Q9C1M7 P37276 Q14204 P38650 Q9JHU4 P36022 Q27171 Q19020 Q9SMH5 Q8IID4 O13290 Q8IBG1 Q96M86
Q8TD57 Q9P225 Q8BW94 Q9MBF8 Q8IVF4 P23098 P39057 Q9NYC9 Q9SMH3 Q9UFH2 Q96DT5 Q69Z23 Q39565 Q96JB1 Q91XQ0 Q8VHE6 Q8TE73 Q39575 Q63164 Q39610 P45444 P45443 P78716 Q923J6 Q3V0Q1 Q6ZR08 Q8NCM8 Q45VK7 Q9JJ79 Q27802 M0R8U1 Q19542 Q9C1M7 P37276 Q14204 P38650 Q9JHU4 P36022 Q27171 Q19020 Q9SMH5 Q8IID4 O13290 Q8IBG1 Q96M86
Pfam
Interpro
IPR003593
AAA+_ATPase
+ More
IPR041466 Dynein_AAA5_ext
IPR042219 AAA_lid_11_sf
IPR004273 Dynein_heavy_D6_P-loop
IPR013602 Dynein_heavy_dom-2
IPR035699 AAA_6
IPR041658 AAA_lid_11
IPR041228 Dynein_C
IPR042228 Dynein_2_C
IPR042222 Dynein_2_N
IPR041589 DNAH3_AAA_lid_1
IPR035706 AAA_9
IPR024743 Dynein_HC_stalk
IPR024317 Dynein_heavy_chain_D4_dom
IPR027417 P-loop_NTPase
IPR026975 DNAH1
IPR026983 DHC_fam
IPR002048 EF_hand_dom
IPR018247 EF_Hand_1_Ca_BS
IPR013594 Dynein_heavy_dom-1
IPR030443 DNAH9
IPR011043 Gal_Oxase/kelch_b-propeller
IPR017868 Filamin/ABP280_repeat-like
IPR011498 Kelch_2
IPR001736 PLipase_D/transphosphatidylase
IPR014756 Ig_E-set
IPR015915 Kelch-typ_b-propeller
IPR002909 IPT_dom
IPR001298 Filamin/ABP280_rpt
IPR013783 Ig-like_fold
IPR026815 DYNC2H1
IPR011704 ATPase_dyneun-rel_AAA
IPR041466 Dynein_AAA5_ext
IPR042219 AAA_lid_11_sf
IPR004273 Dynein_heavy_D6_P-loop
IPR013602 Dynein_heavy_dom-2
IPR035699 AAA_6
IPR041658 AAA_lid_11
IPR041228 Dynein_C
IPR042228 Dynein_2_C
IPR042222 Dynein_2_N
IPR041589 DNAH3_AAA_lid_1
IPR035706 AAA_9
IPR024743 Dynein_HC_stalk
IPR024317 Dynein_heavy_chain_D4_dom
IPR027417 P-loop_NTPase
IPR026975 DNAH1
IPR026983 DHC_fam
IPR002048 EF_hand_dom
IPR018247 EF_Hand_1_Ca_BS
IPR013594 Dynein_heavy_dom-1
IPR030443 DNAH9
IPR011043 Gal_Oxase/kelch_b-propeller
IPR017868 Filamin/ABP280_repeat-like
IPR011498 Kelch_2
IPR001736 PLipase_D/transphosphatidylase
IPR014756 Ig_E-set
IPR015915 Kelch-typ_b-propeller
IPR002909 IPT_dom
IPR001298 Filamin/ABP280_rpt
IPR013783 Ig-like_fold
IPR026815 DYNC2H1
IPR011704 ATPase_dyneun-rel_AAA
ProteinModelPortal
Q9C0G6.3
Q9P2D7.5
E9Q8T7.1
Q8WXX0.2
Q63170.2
P0C6F1.1
+ More
Q8TD57.1 Q9P225.3 Q8BW94.2 Q9MBF8.1 Q8IVF4.4 P23098.1 P39057.1 Q9NYC9.3 Q9SMH3.1 Q9UFH2.3 Q96DT5.4 Q69Z23.2 Q39565.1 Q96JB1.2 Q91XQ0.2 Q8VHE6.2 Q8TE73.3 Q39575.1 Q63164.2 Q39610.2 P45444.2 P45443.1 P78716.1 Q923J6.2 Q3V0Q1.2 Q6ZR08.2 Q8NCM8.4 Q45VK7.1 Q9JJ79.1 Q27802.2 M0R8U1.1 Q19542.2 Q9C1M7.1 P37276.2 Q14204.5 P38650.1 Q9JHU4.2 P36022.1 Q27171.1 Q19020.1 Q9SMH5.2 Q8IID4.1 O13290.1 Q8IBG1.2 Q96M86.2
Q8TD57.1 Q9P225.3 Q8BW94.2 Q9MBF8.1 Q8IVF4.4 P23098.1 P39057.1 Q9NYC9.3 Q9SMH3.1 Q9UFH2.3 Q96DT5.4 Q69Z23.2 Q39565.1 Q96JB1.2 Q91XQ0.2 Q8VHE6.2 Q8TE73.3 Q39575.1 Q63164.2 Q39610.2 P45444.2 P45443.1 P78716.1 Q923J6.2 Q3V0Q1.2 Q6ZR08.2 Q8NCM8.4 Q45VK7.1 Q9JJ79.1 Q27802.2 M0R8U1.1 Q19542.2 Q9C1M7.1 P37276.2 Q14204.5 P38650.1 Q9JHU4.2 P36022.1 Q27171.1 Q19020.1 Q9SMH5.2 Q8IID4.1 O13290.1 Q8IBG1.2 Q96M86.2
PDB
4RH7
E-value=0,
Score=2716
Ontologies
GO
GO:0045503
GO:0007018
GO:0060285
GO:0030286
GO:0051959
GO:0045505
GO:0008569
GO:0005874
GO:0005858
GO:0005524
GO:0030317
GO:0060294
GO:0036159
GO:0003351
GO:0005930
GO:0003777
GO:0036126
GO:0036156
GO:0003341
GO:0007288
GO:0005929
GO:0005829
GO:0005509
GO:0031514
GO:0008017
GO:0030030
GO:0005737
GO:0120135
GO:0097729
GO:0035545
GO:1905419
GO:0061371
GO:0007368
GO:0007611
GO:0120134
GO:0003356
GO:0060411
GO:0060287
GO:0097728
GO:0036157
GO:0036158
GO:0097228
GO:0021670
GO:0007507
GO:0060271
GO:0005881
GO:0072382
GO:0031122
GO:0030428
GO:0000278
GO:0070789
GO:0001411
GO:0005938
GO:0007097
GO:0016887
GO:0015631
GO:0005868
GO:0047496
GO:0051293
GO:0016567
GO:0070062
GO:1905515
GO:0005886
GO:0035721
GO:0061512
GO:0009953
GO:0005794
GO:0030326
GO:0060976
GO:0003774
GO:0045880
GO:0097542
GO:0007030
GO:0021522
GO:0016485
GO:0045177
GO:0030900
GO:0035735
GO:0030182
GO:0007275
GO:0043053
GO:0008104
GO:0060170
GO:0007635
GO:0030512
GO:0097730
GO:0061066
GO:0005816
GO:0000132
GO:0000741
GO:0000070
GO:0000235
GO:0030473
GO:0098958
GO:0048813
GO:0007098
GO:0045169
GO:0007298
GO:0042623
GO:0007052
GO:0007312
GO:0007405
GO:0045198
GO:0050658
GO:0008090
GO:0016319
GO:0040001
GO:0007051
GO:0030723
GO:0035149
GO:0034501
GO:0030071
GO:0008088
GO:0051237
GO:0005875
GO:0051683
GO:0048477
GO:0048134
GO:0007282
GO:0051642
GO:0035011
GO:1904115
GO:1904801
GO:0006886
GO:0046604
GO:0045197
GO:0007279
GO:0000776
GO:0007349
GO:0045478
GO:0007294
GO:0040003
GO:0034063
GO:1990904
GO:0048311
GO:0008298
GO:0097711
GO:0051301
GO:0090235
GO:0032388
GO:0043312
GO:0060236
GO:0120162
GO:0010389
GO:0030175
GO:0035578
GO:0000086
GO:1905832
GO:0033962
GO:0005813
GO:0019886
GO:0003723
GO:0016020
GO:0006888
GO:0005576
GO:0030424
GO:1905243
GO:1990090
GO:0043025
GO:0007286
GO:0002177
GO:0005635
GO:0005819
GO:1990048
GO:0051296
GO:1902473
GO:0000922
GO:1904811
GO:0051932
GO:0048814
GO:0045202
GO:0048489
GO:0051661
GO:0016322
GO:0030990
GO:0072594
GO:0044458
GO:0097014
GO:0051315
GO:0000742
GO:0035974
GO:0007129
GO:0030981
GO:1990758
GO:0030989
GO:1990574
GO:0006813
GO:0006810
GO:0009072
GO:0007169
GO:0016021
Topology
Subcellular location
Cytoplasm
Cytoskeleton
Cilium axoneme
Cell projection
Cilium
Flagellum
Flagellum axoneme
Cell membrane Localizes to the apical cytoplasm (By similarity). According to PubMed:8666668, it localizes to Golgi apparatus, cytoplasmic vesicle and endoplasmic reticulum (PubMed:8666668). With evidence from 4 publications.
Cilium membrane
Flagellum basal body
Flagellum membrane
Microtubule organizing center
Spindle pole body
Length:
3694
Number of predicted TMHs:
0
Exp number of AAs in TMHs:
2.74048000000002
Exp number, first 60 AAs:
0
Total prob of N-in:
0.00170
outside
1 - 3694
Population Genetic Test Statistics
Pi
4.803594
Theta
18.559713
Tajima's D
-1.915554
CLR
0.054187
CSRT
0.0192490375481226
Interpretation
Uncertain
