UniProt | Protein Name |
---|---|
Q9GZR5 |
|
GO Term | Evidence Code | PMID |
---|---|---|
fatty acid elongation, polyunsaturated fatty acid | ||
fatty acid biosynthetic process |
|
|
sphingolipid biosynthetic process | ||
long-chain fatty-acyl-CoA biosynthetic process |
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:13912 | acquired color blindness | |
DOID:1432 | blindness | |
DOID:0050467 | erythrokeratodermia variabilis | |
DOID:0050534 | congenital stationary night blindness | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050635 | alternating hemiplegia of childhood | |
DOID:0050753 | cerebellar ataxia | |
DOID:1441 | autosomal dominant cerebellar ataxia | |
DOID:14501 | Sjogren-Larsson syndrome | |
DOID:0050817 | Stargardt disease |
HPO ID | HPO Term |
---|---|
HP:0007704 | Paroxysmal involuntary eye movements |
HP:0007722 | Retinal pigment epithelial atrophy |
HP:0007754 | Macular dystrophy |
HP:0007772 | Impaired smooth pursuit |
HP:0007814 | Retinal pigment epithelial mottling |
HP:0008002 | Abnormality of macular pigmentation |
HP:0008059 | Aplasia/Hypoplasia of the macula |
HP:0008064 | Ichthyosis |
HP:0010783 | Erythema |
HP:0011003 | High myopia |
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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Last updated: August 19, 2024