UniProt | Protein Name |
---|---|
P22303 |
|
GO Term | Evidence Code | PMID |
---|---|---|
retina development in camera-type eye | ||
acetylcholine catabolic process in synaptic cleft |
|
|
regulation of receptor recycling | ||
positive regulation of protein secretion |
|
|
amyloid precursor protein metabolic process |
|
GO Term | Evidence Code | PMID |
---|---|---|
nucleus | ||
neuromuscular junction | ||
extracellular region | ||
basement membrane |
|
|
synaptic cleft |
GO Term | Evidence Code | PMID |
---|---|---|
acetylcholine binding | ||
hydrolase activity | ||
protein homodimerization activity | ||
amyloid-beta binding |
|
|
laminin binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0110303 | autosomal dominant limb-girdle muscular dystrophy type 1H | |
DOID:0110304 | autosomal dominant limb-girdle muscular dystrophy type 2 | |
DOID:0110305 | autosomal dominant limb-girdle muscular dystrophy type 1 | |
DOID:0110306 | autosomal dominant limb-girdle muscular dystrophy type 3 | |
DOID:0110632 | megaconial type congenital muscular dystrophy | |
DOID:0110633 | rigid spine muscular dystrophy 1 | |
DOID:0110634 | congenital muscular dystrophy 1B | |
DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | |
DOID:0110636 | congenital merosin-deficient muscular dystrophy 1A | |
DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
175074 | WB:WBGene00000038 | ||
175076 | WB:WBGene00000037 | ||
181706 | WB:WBGene00000035 | ||
41625 | FB:FBgn0000024 | ||
100169895 | CIOIN03667 | ||
114549 | ZFIN:ZDB-GENE-010906-1 | DANRE41472 | |
103043295 | ASTMX22063 | ||
108267799 | ICTPU32931 | ||
113580815 | ELEEL27237 | ||
106577883 | SALSA57592 |
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Last updated: August 19, 2024