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:0050635 | alternating hemiplegia of childhood | |
DOID:0050817 | Stargardt disease | |
DOID:0050841 | focal hand dystonia | |
DOID:0060823 | syndromic X-linked intellectual disability 94 | |
DOID:0080348 | Alzheimer's disease 1 | |
DOID:0090103 | Huntington's disease-like 1 | |
DOID:0090104 | Huntington's disease-like 2 | |
DOID:0110035 | Alzheimer's disease 2 | |
DOID:0110037 | Alzheimer's disease 5 | |
DOID:0110038 | Alzheimer's disease 6 |
HPO ID | HPO Term |
---|---|
HP:0003208 | Fingerprint intracellular accumulation of autofluorescent lipopigment storage material |
HP:0003621 | Juvenile onset |
HP:0003657 | Vascular granular osmiophilic material deposition |
HP:0003698 | Difficulty standing |
HP:0003739 | Myoclonic spasms |
HP:0004302 | Functional motor deficit |
HP:0005324 | Disturbance of facial expression |
HP:0005484 | Secondary microcephaly |
HP:0007010 | Poor fine motor coordination |
HP:0007064 | Progressive language deterioration |
Disease ID | Disease Name |
---|---|
ORPHA:168491 |
|
OMIM:256730 |
|
ORPHA:79263 |
|
ORPHA:79264 |
|
ORPHA:79262 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
29411 | RGD:61994 | RATNO34701 | |
100720295 | CAVPO23603 | ||
101560928 | OCTDE19791 | ||
101718692 | HETGA26200 | ||
101868444 | MELUD20068 | ||
100032080 | MONDO22911 | ||
102450927 | PELSI01471 | ||
100563048 | ANOCA13148 | ||
103682394 | URSMA32745 | ||
114044932 | VOMUR17720 |
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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