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:0050981 | spinocerebellar ataxia type 34 | |
DOID:0060319 | cardiac arrest | |
DOID:0060320 | inguinal hernia | |
DOID:0060655 | autosomal recessive congenital ichthyosis | |
DOID:0060656 | autosomal recessive congenital ichthyosis 1 | |
DOID:0110384 | retinitis pigmentosa 25 | |
DOID:0110406 | retinitis pigmentosa 30 | |
DOID:0110870 | congenital stationary night blindness 1A | |
DOID:0111005 | cone-rod dystrophy 2 | |
DOID:0111012 | cone-rod dystrophy 7 |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000007 | Autosomal recessive inheritance |
HP:0000023 | Inguinal hernia |
HP:0000230 | Gingivitis |
HP:0000252 | Microcephaly |
HP:0000324 | Facial asymmetry |
HP:0000486 | Strabismus |
HP:0000493 | Abnormal foveal morphology |
HP:0000505 | Visual impairment |
HP:0000551 | Color vision defect |
Disease ID | Disease Name |
---|---|
ORPHA:1955 |
|
OMIM:133190 |
|
OMIM:614457 |
|
OMIM:600110 |
|
ORPHA:827 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
123797477 | URSAM04941 | ||
100475550 | AILME15808 | ||
101677575 | MUSPF13446 | ||
101101313 | FELCA11137 | ||
122220121 | PANLE16372 | ||
118905067 | BALMU27496 | ||
100654940 | LOXAF20790 | ||
100069512 | HORSE00672 | ||
100511670 | PIGXX13926 | ||
532015 | BOVIN35379 |
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Last updated: August 19, 2024