UniProt | Protein Name |
---|---|
P50897 |
|
GO Term | Evidence Code | PMID |
---|---|---|
neurotransmitter secretion | ||
negative regulation of apoptotic process | ||
brain development | ||
positive regulation of pinocytosis | ||
nervous system development |
GO Term | Evidence Code | PMID |
---|---|---|
lysophosphatidic acid binding | ||
sulfatide binding | ||
palmitoyl-(protein) hydrolase activity | ||
protein binding | ||
long-chain acyl-CoA hydrolase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:1324 | lung cancer | |
DOID:13548 | secondary Parkinson disease | |
DOID:1432 | blindness | |
DOID:1443 | cerebral degeneration | |
DOID:14503 | neuronal ceroid lipofuscinosis | |
DOID:14525 | Reye syndrome | |
DOID:1470 | major depressive disorder | |
DOID:1595 | melancholic depression | |
DOID:1596 | depressive disorder | |
DOID:1612 | breast cancer |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000253 | Progressive microcephaly |
HP:0000483 | Astigmatism |
HP:0000529 | Progressive visual loss |
HP:0000543 | Optic disc pallor |
HP:0000545 | Myopia |
HP:0000546 | Retinal degeneration |
HP:0000550 | Undetectable electroretinogram |
HP:0000572 | Visual loss |
HP:0000580 | Pigmentary retinopathy |
Disease ID | Disease Name |
---|---|
ORPHA:168491 |
|
OMIM:256730 |
|
ORPHA:79263 |
|
ORPHA:79264 |
|
ORPHA:79262 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115175965 | SALTR03990 | ||
115535255 | GADMO35594 | ||
101166727 | ORYLA02045 | ||
100710936 | ORENI42018 | ||
115579253 | SPAAU22476 | ||
115579256 | SPAAU22476 | ||
100036952 | Xenbase:XB-GENE-17335881 | ||
100037210 | Xenbase:XB-GENE-6254984 | ||
448650 | Xenbase:XB-GENE-923070 | ||
101942757 | CHRPI15299 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024