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:0050981 | spinocerebellar ataxia type 34 | |
DOID:0060319 | cardiac arrest | |
DOID:0060320 | inguinal hernia | |
DOID:0060655 | autosomal recessive congenital ichthyosis | |
DOID:0060656 | autosomal recessive congenital ichthyosis 1 | |
DOID:0110384 | retinitis pigmentosa 25 | |
DOID:0110406 | retinitis pigmentosa 30 | |
DOID:0110870 | congenital stationary night blindness 1A | |
DOID:0111005 | cone-rod dystrophy 2 | |
DOID:0111012 | cone-rod dystrophy 7 |
HPO ID | HPO Term |
---|---|
HP:0001288 | Gait disturbance |
HP:0001347 | Hyperreflexia |
HP:0001510 | Growth delay |
HP:0002066 | Gait ataxia |
HP:0002070 | Limb ataxia |
HP:0002073 | Progressive cerebellar ataxia |
HP:0002075 | Dysdiadochokinesis |
HP:0002080 | Intention tremor |
HP:0002099 | Asthma |
HP:0002120 | Cerebral cortical atrophy |
Disease ID | Disease Name |
---|---|
ORPHA:1955 |
|
OMIM:133190 |
|
OMIM:614457 |
|
OMIM:600110 |
|
ORPHA:827 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
102172444 | CAPHI29818 | ||
100353429 | RABIT02611 | ||
100774858 | CRIGR06812 | ||
83603 | MGI:1933331 | MOUSE61150 | |
315851 | RGD:1305630 | RATNO41181 | |
100720101 | CAVPO03094 | ||
101572820 | OCTDE13264 | ||
101876966 | MELUD01970 | ||
100017828 | MONDO11206 | ||
102446236 | PELSI12501 |
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Last updated: August 19, 2024