myosin VIIA
| UniProt | Protein Name |
|---|---|
| Q13402 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| phagolysosome assembly | ||
| intracellular protein transport | ||
| endocytosis | ||
| actin filament organization | ||
| lysosome organization |
| GO Term | Evidence Code | PMID |
|---|---|---|
| apical plasma membrane | ||
| myosin VII complex | ||
| photoreceptor connecting cilium | ||
| stereocilium | ||
| melanosome |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein domain specific binding | ||
| spectrin binding | ||
| identical protein binding | ||
| ADP binding | ||
| actin filament binding |
| Gene Ontology |
|---|
| ATP binding |
| actin binding |
| cytoskeletal motor activity |
| nucleotide binding |
| 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:9649 | congenital nystagmus |
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 4647 | Xenbase:XB-GENE-494060 | ||
| 4648 | WB:WBGene00002039 | ||
| 17921 | MOUSE54674 | ||
| 17922 | WB:WBGene00002039 | ||
| 266714 | RATNO15521 | ||
| 397373 | PIGXX35055 | ||
| 485174 | CANLF08243 | ||
| 699411 | MACMU11296 | ||
| 100063344 | HORSE39759 | ||
| 100084198 | ORNAN13257 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: December 8, 2025