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: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 |
---|---|---|---|
106608940 | SALSA136114 | ||
115194622 | SALTR89909 | ||
115198571 | SALTR64885 | ||
115529722 | GADMO21561 | ||
100697913 | ORENI52376 | ||
100158421 | Xenbase:XB-GENE-923165 | ||
108703508 | Xenbase:XB-GENE-17330311 | ||
100490673 | Xenbase:XB-GENE-923160 | ||
101954077 | CHRPI28870 | ||
113454074 | PSETE27442 |
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Last updated: August 19, 2024