GO Term | Evidence Code | PMID |
---|---|---|
chromatin remodeling | ||
protein phosphorylation | ||
cytoskeleton organization | ||
cytoskeleton organization | ||
brain development |
GO Term | Evidence Code | PMID |
---|---|---|
magnesium ion binding | ||
protein serine/threonine kinase activity | ||
protein serine/threonine kinase activity | ||
3-phosphoinositide-dependent protein kinase activity | ||
DNA-dependent protein kinase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:0111403 | mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
22983 | Xenbase:XB-GENE-1006519 | HUMAN41174 | |
23031 | FB:FBgn0267390 | ||
56527 | Xenbase:XB-GENE-1006519 | ||
328329 | FB:FBgn0267390 | ||
353118 | RATNO15226 | ||
375449 | FB:FBgn0267390 | ||
456367 | PANTR17326 | ||
539825 | BOVIN32496 | ||
546071 | FB:FBgn0267390 | ||
717903 | MACMU20870 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 7, 2025