GO Term | Evidence Code | PMID |
---|---|---|
eye morphogenesis | ||
protein glycosylation | ||
O-glycan processing |
GO Term | Evidence Code | PMID |
---|---|---|
Golgi membrane | ||
Golgi apparatus | ||
membrane | ||
secretory vesicle |
GO Term | Evidence Code | PMID |
---|---|---|
glycosyltransferase activity | ||
carbohydrate binding | ||
acetylglucosaminyltransferase activity | ||
metal ion binding | ||
hexosyltransferase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050453 | lissencephaly | |
DOID:0050560 | Walker-Warburg syndrome | |
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | |
DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | |
DOID:0112378 | muscular dystrophy-dystroglycanopathy type B3 | |
DOID:10584 | retinitis pigmentosa | |
DOID:9884 | muscular dystrophy |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: February 17, 2025