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:13909 | red-green color blindness | |
DOID:13910 | red color blindness | |
DOID:13911 | achromatopsia | |
DOID:14791 | Leber congenital amaurosis | |
DOID:1555 | urticaria | |
DOID:1558 | angioedema | |
DOID:1588 | thrombocytopenia | |
DOID:162 | cancer | |
DOID:1697 | ichthyosis | |
DOID:1699 | obsolete congenital ichthyosiform erythroderma |
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 |
---|---|---|---|
116821636 | CHEAB25005 | ||
109531419 | HIPCM23800 | ||
105295295 | PTEVA04238 | ||
115044550 | ECHNA26585 | ||
115396671 | SALFA31537 | ||
103388604 | CYNSE06518 | ||
105517657 | COLAP30887 | ||
105811768 | PROCO06014 | ||
851087 | SGD:S000004364 | ||
109078047 | CYPCA34318 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024