Pre Gene Modal
BGIBMGA001403
Annotation
PREDICTED:_uncharacterized_protein_LOC106129089_isoform_X2_[Amyelois_transitella]
Full name
Centrosomal protein of 120 kDa
Alternative Name
Coiled-coil domain-containing protein 100
Location in the cell
Cytoplasmic   Reliability : 1.887 Nuclear   Reliability : 2.268
Sequence
CDS
ATGTACTTACTGGAGCCCGTCGTTTTGGAGACGAGCAAAAGCGACACGTGCATCACAAGTCCTAAACGGGCCGCCCGTAAAGACAATCACACAGATTTGGTGAAAATGGCGCTATCGGAAGCCGACCGCGACAGCATCATGCGGAGGTTCGTGGACGAGCTGGAAGACTGGAAGGAGAAGCAGCAGGAGCTGCACAAACTGCAGTTGAAGCGCAAAGAAGAGTACCATTTAGAGCTATTGGCCAAGGAGTGGGCCAAGCAGCGCGTGGAGCTGGAGTGCCGGCTGGCGAGGGGCATCGAGCAGTGCCGCGCCCTCGCCGCCGACCTCGCCGCCGCCACAGACGACTTCAGGGCGAGGGGACACAGGAACTCCGAGAGGGAGAAGAAGTTATTGGAAGCGAAGAAAGCTTTAGAAGCGCATTACACAGCCAAGTACCAGGAGTTGAGAGAGGCCTCATTAAAAATGGAGGACGACATGAATCATCAGCTGAAAGTCAAGGACATGAGGATCGAAGAGCTGGAGCTTAAAATAATGCAGCTTGAGAAACAGGTGGACGTTTTGAAGAATACCATGAAGGACATTGAGAAAGAAGCCGAAACCCGATATTCTGGTCTAACTAAAGATCAAACTGCGAGTCTCATACAAGAATTGAGATGTTTAGAAGAAAAACTAGATAGTGCGGTCCAATCGAAAGCGTTCTTCAAAGAGCAGTGGGGCCGCGCTGTCAGGGAACTGCACCTGCTGAAGCTGGACACCAGGAAGCAAATGTTGTCGCAGCTGCAGCAGGACAGGAGGGAGCTGGGTGATGCTGGTTTAGACACAATAATAGATGACAACGAAAGTAAACGCAATCAAGATGCGATGGACATTAAAAAATTGAAAGACGATTTTTATGTTGACATTTTAGCGAGCACACCGGCACTGGAAATCGATTCGTTCATCACCACATCTGGTTCGGGTGTTGTAGAAATGTTTGACGATTTAAGAAGCGTCGTTAAGAACCCGATAAATGATAAACTAAACAAATTGATATCACAACGCGATCGGCTCATACAGGACGAGAATCCGAATGAAGAACTTCTGAAGCAATTGAACCAGGAAATTAGAAGTATCCTATTAAACTGTGGCTCCTGA
Protein
MYLLEPVVLETSKSDTCITSPKRAARKDNHTDLVKMALSEADRDSIMRRFVDELEDWKEKQQELHKLQLKRKEEYHLELLAKEWAKQRVELECRLARGIEQCRALAADLAAATDDFRARGHRNSEREKKLLEAKKALEAHYTAKYQELREASLKMEDDMNHQLKVKDMRIEELELKIMQLEKQVDVLKNTMKDIEKEAETRYSGLTKDQTASLIQELRCLEEKLDSAVQSKAFFKEQWGRAVRELHLLKLDTRKQMLSQLQQDRRELGDAGLDTIIDDNESKRNQDAMDIKKLKDDFYVDILASTPALEIDSFITTSGSGVVEMFDDLRSVVKNPINDKLNKLISQRDRLIQDENPNEELLKQLNQEIRSILLNCGS
Summary
Description
Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors and for proper positioning of neurons during brain development. Also implicated in the migration and selfrenewal of neural progenitors. Required for centriole duplication and maturation during mitosis and subsequent ciliogenesis. Required for the recruitment of CEP295 to the proximal end of new-born centrioles at the centriolar microtubule wall during early S phase in a PLK4-dependent manner (By similarity).
Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors and for proper positioning of neurons during brain development. Also implicated in the migration and selfrenewal of neural progenitors. Required for centriole duplication and maturation during mitosis and subsequent ciliogenesis (By similarity). Required for the recruitment of CEP295 to the proximal end of new-born centrioles at the centriolar microtubule wall during early S phase in a PLK4-dependent manner (PubMed:27185865).
Plays a role in the microtubule-dependent coupling of the nucleus and the centrosome. Involved in the processes that regulate centrosome-mediated interkinetic nuclear migration (INM) of neural progenitors and for proper positioning of neurons during brain development. Also implicated in the migration and selfrenewal of neural progenitors. May play a role in centriole duplication during mitosis (By similarity). Required for the recruitment of CEP295 to the proximal end of new-born centrioles at the centriolar microtubule wall during early S phase in a PLK4-dependent manner (By similarity).
Subunit
Interacts with TACC2, TACC3, CCDC52, TALPID3.
Interacts with TACC2 and TACC3. Interacts with CCDC52.
Similarity
Belongs to the CEP120 family.
Keywords
3D-structure
Alternative splicing
Coiled coil
Complete proteome
Cytoplasm
Cytoskeleton
Phosphoprotein
Reference proteome
Ciliopathy
Disease mutation
Joubert syndrome
Polymorphism
Feature
chain Centrosomal protein of 120 kDa
splice variant In isoform 4.
sequence variant In JBTS31; unknown pathological significance.
Ontologies
Topology
Number of predicted TMHs:
0
Exp number of AAs in TMHs:
0.00093
Exp number, first 60 AAs:
0
Total prob of N-in:
0.00108
Population Genetic Test Statistics