UniProt | Protein Name |
---|---|
A0A384P5J0 |
|
O60760 |
|
GO Term | Evidence Code | PMID |
---|---|---|
glutathione metabolic process | ||
locomotory behavior |
|
|
prostaglandin biosynthetic process | ||
signal transduction |
|
|
prostaglandin metabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
cytosol | ||
cytoplasm |
|
|
nucleoplasm |
GO Term | Evidence Code | PMID |
---|---|---|
magnesium ion binding | ||
protein homodimerization activity | ||
calcium ion binding | ||
protein binding | ||
prostaglandin-D synthase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110048 | Alzheimer's disease 15 | |
DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy | |
DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | |
DOID:0110275 | autosomal recessive limb-girdle muscular dystrophy type 2A | |
DOID:0110276 | autosomal recessive limb-girdle muscular dystrophy type 2B | |
DOID:0110277 | autosomal recessive limb-girdle muscular dystrophy type 2C | |
DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | |
DOID:0110279 | autosomal recessive limb-girdle muscular dystrophy type 2E | |
DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | |
DOID:0110281 | autosomal recessive limb-girdle muscular dystrophy type 2G |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
379417 | Xenbase:XB-GENE-944784 | ||
398969 | Xenbase:XB-GENE-6254910 | ||
448666 | Xenbase:XB-GENE-944778 | ||
101943956 | CHRPI02685 | ||
109322344 | CROPO11757 | ||
100399167 | CALJA28797 | ||
105572356 | CERAT40014 | ||
102131661 | MACFA34256 | ||
705227 | MACMU36448 | ||
105479614 | MACNE18308 |
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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