GO Term | Evidence Code | PMID |
---|---|---|
protein O-linked mannosylation |
GO Term | Evidence Code | PMID |
---|---|---|
Golgi apparatus | ||
rough endoplasmic reticulum |
GO Term | Evidence Code | PMID |
---|---|---|
molecular_function |
Location | References |
---|---|
DO ID | Disease Name | Source |
---|---|---|
DOID:0050560 | Walker-Warburg syndrome | |
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | |
DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | |
DOID:0111241 | congenital muscular dystrophy-dystroglycanopathy type A5 | |
DOID:11724 | limb-girdle muscular dystrophy | |
DOID:12930 | dilated cardiomyopathy | |
DOID:9884 | muscular dystrophy |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
571426 | ZFIN:ZDB-GENE-070412-4 | ||
100145309 | Xenbase:XB-GENE-964270 | ||
79147 | HGNC:17997 | ||
243853 | MGI:2447586 | ||
308390 | RGD:1305852 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024