GO Term | Evidence Code | PMID |
---|---|---|
brain development | ||
protein O-linked glycosylation | ||
skeletal muscle fiber differentiation | ||
biological_process | ||
basement membrane organization |
GO Term | Evidence Code | PMID |
---|---|---|
nucleus | ||
cis-Golgi network | ||
endoplasmic reticulum | ||
Golgi apparatus | ||
Golgi membrane |
GO Term | Evidence Code | PMID |
---|---|---|
phosphotransferase activity, for other substituted phosphate groups |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050559 | Fukuyama congenital muscular dystrophy | |
DOID:0050560 | Walker-Warburg syndrome | |
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | |
DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | |
DOID:0110443 | dilated cardiomyopathy 1B | |
DOID:0110444 | dilated cardiomyopathy 1X | |
DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | |
DOID:9884 | muscular dystrophy |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100693284 | ORENI66974 | ||
115592768 | SPAAU33607 | ||
100124956 | Xenbase:XB-GENE-971788 | ||
101942066 | CHRPI16935 | ||
109323584 | CROPO13036 | ||
113448026 | PSETE21620 | ||
100545765 | MELGA13647 | ||
103823235 | SERCA20200 | ||
100076185 | ORNAN32450 | ||
100405050 | CALJA18845 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024