GO Term | Evidence Code | PMID |
---|---|---|
protein deglycosylation | ||
biological_process | ||
brain development | ||
skeletal muscle fiber differentiation | ||
cerebellar cortex development |
GO Term | Evidence Code | PMID |
---|---|---|
Golgi apparatus | ||
Golgi membrane | ||
endoplasmic reticulum | ||
cis-Golgi network | ||
nucleus |
GO Term | Evidence Code | PMID |
---|---|---|
phosphotransferase activity, for other substituted phosphate groups |
Gene Ontology |
---|
glycoprotein metabolic process |
InterPro |
---|
LicD family |
Ribitol-5-phosphate transferase FKTN, N-terminal |
Ribitol-5-phosphate transferase FKTN-related |
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 | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
2218 | HGNC:3622 | HUMAN97902 | ||
173469 | WB:WBGene00020307 | |||
188207 | WB:WBGene00011554 | |||
189104 | WB:WBGene00020924 | |||
189107 | WB:WBGene00020927 | |||
189504 | WB:WBGene00021249 | |||
246179 | 10090_1:00111c | MGI:2179507 | MOUSE43139 | |
464634 | PANTR44522 | |||
481652 | CANLF02398 | |||
712201 | MACMU11815 |
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GlyCosmos Portal v4.1.0
Last updated: December 9, 2024