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:0060814 | Wilson-Turner syndrome | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0070123 | congenital nongoitrous hypothyroidism 4 | |
DOID:0070124 | congenital nongoitrous hypothyroidism 2 | |
DOID:0070125 | congenital nongoitrous hypothyroidism 5 | |
DOID:0070126 | congenital nongoitrous hypothyroidism 1 | |
DOID:0070127 | congenital nongoitrous hypothyroidism 3 | |
DOID:0070128 | congenital nongoitrous hypothyroidism 6 |
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