UniProt | Protein Name |
---|---|
P22303 |
|
GO Term | Evidence Code | PMID |
---|---|---|
osteoblast development | ||
negative regulation of synaptic transmission, cholinergic | ||
acetylcholine catabolic process | ||
cell adhesion |
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:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | |
DOID:0110281 | autosomal recessive limb-girdle muscular dystrophy type 2G | |
DOID:0110282 | autosomal recessive limb-girdle muscular dystrophy type 2H | |
DOID:0110283 | autosomal recessive limb-girdle muscular dystrophy type 2J | |
DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | |
DOID:0110285 | autosomal recessive limb-girdle muscular dystrophy type 2Q | |
DOID:0110286 | obsolete autosomal recessive limb-girdle muscular dystrophy type 2R | |
DOID:0110287 | autosomal recessive limb-girdle muscular dystrophy type 2S | |
DOID:0110289 | autosomal recessive limb-girdle muscular dystrophy type 2Y | |
DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O |
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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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024