UniProt | Protein Name |
---|---|
Q9GZR5 |
|
GO Term | Evidence Code | PMID |
---|---|---|
fatty acid elongation, monounsaturated fatty acid | ||
unsaturated fatty acid biosynthetic process | ||
detection of visible light | ||
very long-chain fatty acid biosynthetic process | ||
fatty acid elongation, saturated fatty acid |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum | ||
endoplasmic reticulum membrane |
GO Term | Evidence Code | PMID |
---|---|---|
G protein-coupled photoreceptor activity |
|
|
protein binding | ||
fatty acid elongase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:13912 | acquired color blindness | |
DOID:1432 | blindness | |
DOID:0050467 | erythrokeratodermia variabilis | |
DOID:0050534 | congenital stationary night blindness | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050635 | alternating hemiplegia of childhood | |
DOID:0050753 | cerebellar ataxia | |
DOID:1441 | autosomal dominant cerebellar ataxia | |
DOID:14501 | Sjogren-Larsson syndrome | |
DOID:0050817 | Stargardt disease |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000007 | Autosomal recessive inheritance |
HP:0000023 | Inguinal hernia |
HP:0000230 | Gingivitis |
HP:0000252 | Microcephaly |
HP:0000324 | Facial asymmetry |
HP:0000486 | Strabismus |
HP:0000493 | Abnormal foveal morphology |
HP:0000505 | Visual impairment |
HP:0000551 | Color vision defect |
Disease ID | Disease Name |
---|---|
ORPHA:1955 |
|
OMIM:133190 |
|
OMIM:614457 |
|
OMIM:600110 |
|
ORPHA:827 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
39245 | FB:FBgn0036128 | ||
317841 | FB:FBgn0052072 | ||
619277 | CIOIN02486 | ||
103186183 | CALMI34037 | ||
102364316 | LATCH04543 | ||
393769 | ZFIN:ZDB-GENE-040426-1767 | DANRE11209 | |
335732 | ZFIN:ZDB-GENE-030131-7672 | ||
103035050 | ASTMX11422 | ||
108272628 | ICTPU14393 | ||
113572917 | ELEEL03574 |
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Last updated: August 19, 2024