UniProt | Protein Name |
---|---|
A0A0A0MRF5 |
|
Q8IXJ6 |
|
GO Term | Evidence Code | PMID |
---|---|---|
subtelomeric heterochromatin formation | ||
positive regulation of DNA binding | ||
proteasome-mediated ubiquitin-dependent protein catabolic process | ||
regulation of phosphorylation | ||
epigenetic regulation of gene expression |
GO Term | Evidence Code | PMID |
---|---|---|
glial cell projection | ||
microtubule | ||
heterochromatin | ||
lateral loop | ||
spindle |
GO Term | Evidence Code | PMID |
---|---|---|
NAD+ ADP-ribosyltransferase activity | ||
transcription factor binding | ||
NAD-dependent histone deacetylase activity | ||
zinc ion binding | ||
chromatin binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110277 | autosomal recessive limb-girdle muscular dystrophy type 2C | |
DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | |
DOID:0110279 | autosomal recessive limb-girdle muscular dystrophy type 2E | |
DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | |
DOID:0110281 | autosomal recessive limb-girdle muscular dystrophy type 2G | |
DOID:0110282 | autosomal recessive limb-girdle muscular dystrophy type 2H | |
DOID:0110283 | autosomal recessive limb-girdle muscular dystrophy type 2J | |
DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | |
DOID:0110285 | autosomal recessive limb-girdle muscular dystrophy type 2Q | |
DOID:0110286 | obsolete autosomal recessive limb-girdle muscular dystrophy type 2R |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
495688 | Xenbase:XB-GENE-987378 | ||
100489469 | Xenbase:XB-GENE-987375 | ||
101948487 | CHRPI19923 | ||
113445924 | PSETE19026 | ||
103166548 | ORNAN23038 | ||
100393634 | CALJA24384 | ||
100425019 | MACMU18361 | ||
100997912 | PAPAN23744 | ||
101148685 | GORGO17325 | ||
100172430 | PONAB14186 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 19, 2024