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:11661 | blue color blindness | |
DOID:11771 | spontaneous ocular nystagmus | |
DOID:11832 | visual epilepsy | |
DOID:11847 | coronary thrombosis | |
DOID:12697 | locked-in syndrome | |
DOID:12835 | quadriplegia | |
DOID:1289 | neurodegenerative disease | |
DOID:13072 | acquired hyperkeratosis | |
DOID:13174 | dissociated nystagmus | |
DOID:13399 | color blindness |
HPO ID | HPO Term |
---|---|
HP:0000966 | Hypohidrosis |
HP:0001019 | Erythroderma |
HP:0001025 | Urticaria |
HP:0001250 | Seizure |
HP:0001251 | Ataxia |
HP:0001257 | Spasticity |
HP:0001260 | Dysarthria |
HP:0001263 | Global developmental delay |
HP:0001265 | Hyporeflexia |
HP:0001272 | Cerebellar atrophy |
Disease ID | Disease Name |
---|---|
ORPHA:1955 |
|
OMIM:133190 |
|
OMIM:614457 |
|
OMIM:600110 |
|
ORPHA:827 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115566768 | SPAAU59875 | ||
108717990 | Xenbase:XB-GENE-6486190 | ||
121393919 | Xenbase:XB-GENE-17332749 | ||
101732387 | Xenbase:XB-GENE-5892987 | ||
101945122 | CHRPI34630 | ||
109311815 | CROPO09975 | ||
116240605 | PHACC00267 | ||
100081381 | ORNAN10577 | ||
100396385 | CALJA30685 | ||
105588064 | CERAT26786 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024