UniProt | Protein Name |
---|---|
Q5XIN7 |
|
A0A8I6AMP8 |
|
A6JZ66 |
|
GO Term | Evidence Code | PMID |
---|---|---|
brain development | ||
protein O-linked glycosylation | ||
protein modification process | ||
protein glycosylation | ||
protein O-linked mannosylation |
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 |
---|---|---|---|---|
101998301 | 79684_0:004b85 | |||
102022683 | 34839_0:002f66 | CHILA15879 | ||
102177679 | CAPHI21626 | |||
102927351 | 230844_0:000bb6 | |||
103031352 | ASTMX11543 | |||
103182759 | CALMI25672 | |||
103224896 | CHLSB08932 | |||
103272134 | CARSF21511 | |||
103670761 | URSMA14982 | |||
103730307 | 1026970_0:000c87 | NANGA22552 |
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GlyCosmos Portal v4.1.0
Last updated: December 9, 2024