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:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | |
DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | |
DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | |
DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | |
DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | |
DOID:0110300 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1A | |
DOID:0110301 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1B | |
DOID:0110302 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1C | |
DOID:0110303 | autosomal dominant limb-girdle muscular dystrophy type 1H | |
DOID:0110304 | autosomal dominant limb-girdle muscular dystrophy type 2 |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100353701 | RABIT05217 | ||
105995855 | DIPOR14096 | ||
100768035 | CRIGR05394 | ||
54486 | MGI:1859384 | MOUSE49816 | |
58962 | RGD:69251 | RATNO29904 | |
100734640 | CAVPO10839 | ||
101706734 | HETGA22045 | ||
100016454 | MONDO25678 | ||
102450743 | PELSI13634 | ||
103677906 | URSMA17887 |
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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