UniProt | Protein Name |
---|---|
Q7Z3S7 |
|
GO Term | Evidence Code | PMID |
---|---|---|
detection of light stimulus involved in visual perception | ||
calcium ion transmembrane transport |
GO Term | Evidence Code | PMID |
---|---|---|
voltage-gated calcium channel complex |
GO Term | Evidence Code | PMID |
---|---|---|
voltage-gated calcium channel activity | ||
metal ion binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050534 | congenital stationary night blindness | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050795 | cone dystrophy | |
DOID:0060224 | atrial fibrillation | |
DOID:0081023 | retinal cone dystrophy 4 | |
DOID:0110870 | congenital stationary night blindness 1A | |
DOID:0111005 | cone-rod dystrophy 2 | |
DOID:10141 | obsolete asthenopia | |
DOID:10930 | borderline personality disorder | |
DOID:11661 | blue color blindness |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000486 | Strabismus |
HP:0000505 | Visual impairment |
HP:0000540 | Hypermetropia |
HP:0000545 | Myopia |
HP:0000548 | Cone/cone-rod dystrophy |
HP:0000551 | Color vision defect |
HP:0000613 | Photophobia |
HP:0000639 | Nystagmus |
HP:0000662 | Nyctalopia |
Disease ID | Disease Name |
---|---|
ORPHA:215 |
|
OMIM:610478 |
|
ORPHA:1872 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
114039545 | VOMUR27229 | ||
100964583 | OTOGA07274 | ||
102026185 | CHILA13772 | ||
108235065 | KRYMA09481 | ||
105733745 | AOTNA37571 | ||
101038775 | SAIBB23808 | ||
108420389 | PYGNA04015 | ||
101960125 | ICTTR12028 | ||
103146499 | POEFO13255 | ||
103149375 | POEFO16352 |
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Last updated: August 19, 2024