GO Term | Evidence Code | PMID |
---|---|---|
eye morphogenesis | ||
protein glycosylation | ||
O-glycan processing |
GO Term | Evidence Code | PMID |
---|---|---|
membrane | ||
Golgi apparatus | ||
secretory vesicle | ||
Golgi membrane |
GO Term | Evidence Code | PMID |
---|---|---|
metal ion binding | ||
manganese ion binding | ||
beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase activity | ||
transferase activity | ||
acetylglucosaminyltransferase 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 |
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
108441728 | 42514_0:005890 | |||
108535632 | RHIBE09720 | |||
108891085 | 8187_0:003f97 | |||
108935322 | 113540_1:002869 | |||
109044861 | 7962_0:006472 | CYPCA46450 | ||
109307427 | CROPO14044 | |||
109515106 | 109280_0:0012b2 | |||
109523457 | 109280_0:002a9d | |||
109643457 | 8255_1:004881 | |||
109898153 | 8019_0:0033e5 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024