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:0002123 | Generalized myoclonic seizure |
HP:0002167 | Abnormality of speech or vocalization |
HP:0002187 | Intellectual disability, profound |
HP:0002188 | Delayed CNS myelination |
HP:0002380 | Fasciculations |
HP:0002509 | Limb hypertonia |
HP:0002510 | Spastic tetraplegia |
HP:0002977 | Aplasia/Hypoplasia involving the central nervous system |
HP:0003011 | Abnormality of the musculature |
HP:0003477 | Peripheral axonal neuropathy |
Disease ID | Disease Name |
---|---|
ORPHA:1955 |
|
OMIM:133190 |
|
OMIM:614457 |
|
OMIM:600110 |
|
ORPHA:827 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
105730554 | AOTNA08744 | ||
101034271 | SAIBB05929 | ||
111227693 | SERDU09826 | ||
108434897 | PYGNA18669 | ||
116322620 | OREAU21606 | ||
103135593 | POEFO00044 | ||
103136405 | POEFO00044 | ||
118314073 | SCOMX16644 | ||
102430517 | MYOLU06006 | ||
117020585 | RHIFE11561 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024