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:37 | skin disease | |
DOID:3777 | granuloma annulare | |
DOID:4448 | macular degeneration | |
DOID:4702 | mongolian spot | |
DOID:539 | ophthalmoplegia | |
DOID:540 | strabismus | |
DOID:5614 | eye disease | |
DOID:5844 | myocardial infarction | |
DOID:5854 | silent myocardial infarction | |
DOID:684 | hepatocellular carcinoma |
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 |
---|---|---|---|
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