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:1826 | epilepsy | |
DOID:1837 | diabetic ketoacidosis | |
DOID:2007 | degeneration of macula and posterior pole | |
DOID:2566 | corneal dystrophy | |
DOID:2734 | keratosis follicularis | |
DOID:2738 | pseudoxanthoma elasticum | |
DOID:2752 | glycogen storage disease II | |
DOID:2786 | cerebellar disease | |
DOID:331 | central nervous system disease | |
DOID:3571 | liver cancer |
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 |
---|---|---|---|
109098404 | CYPCA58415 | ||
103729172 | NANGA21985 | ||
116442178 | CORMO19188 | ||
115609845 | STRHB17005 | ||
108309868 | CEBIM15378 |
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Last updated: August 19, 2024