UniProt | Protein Name |
---|---|
Q13402 |
|
GO Term | Evidence Code | PMID |
---|---|---|
pigment granule transport | ||
eye photoreceptor cell development | ||
cochlea development | ||
intracellular protein transport | ||
actin filament-based movement |
GO Term | Evidence Code | PMID |
---|---|---|
photoreceptor inner segment | ||
stereocilium base | ||
upper tip-link density | ||
synapse | ||
cytosol |
GO Term | Evidence Code | PMID |
---|---|---|
protein binding | ||
microfilament motor activity | ||
actin filament binding | ||
spectrin binding | ||
calmodulin binding |
Gene Ontology |
---|
ATP binding |
actin binding |
actin filament binding |
cytoskeletal motor activity |
nucleotide binding |
InterPro |
---|
Kinesin motor domain superfamily |
Myosin head, motor domain |
P-loop containing nucleoside triphosphate hydrolase |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050439 | Usher syndrome | |
DOID:0110477 | autosomal recessive nonsyndromic deafness 2 | |
DOID:0110543 | autosomal dominant nonsyndromic deafness 11 | |
DOID:0110826 | Usher syndrome type 1 | |
DOID:10003 | sensorineural hearing loss | |
DOID:14791 | Leber congenital amaurosis | |
DOID:2742 | auditory system disease | |
DOID:9649 | congenital nystagmus |
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
108263906 | ICTPU27982 | |||
108708815 | Xenbase:XB-GENE-17338023 | |||
109306838 | CROPO03839 | |||
113486388 | ATHCN01958 | |||
113576953 | ELEEL18975 | |||
113905465 | BOBOX35016 | |||
114032744 | VOMUR14533 | |||
114595563 | PODMU19342 | |||
115163305 | SALTR98703 | |||
115206246 | SALTR113216 |
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Last updated: December 9, 2024