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 |
---|---|---|
ubiquitin binding | ||
NAD-dependent protein deacetylase activity | ||
NAD+-protein ADP-ribosyltransferase activity |
|
|
NAD-dependent protein demyristoylase activity | ||
NAD-dependent protein depalmitoylase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110287 | autosomal recessive limb-girdle muscular dystrophy type 2S | |
DOID:0110289 | autosomal recessive limb-girdle muscular dystrophy type 2Y | |
DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | |
DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P | |
DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | |
DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | |
DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | |
DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | |
DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | |
DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I |
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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Last updated: August 19, 2024