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:8499 | night blindness | |
DOID:863 | nervous system disease | |
DOID:9306 | mechanical strabismus | |
DOID:9351 | diabetes mellitus | |
DOID:9352 | type 2 diabetes mellitus | |
DOID:9408 | acute myocardial infarction | |
DOID:9649 | congenital nystagmus | |
DOID:9650 | pathologic nystagmus | |
DOID:9837 | hypertropia |
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 |
---|---|---|---|
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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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024