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 |
---|---|---|
paranodal junction | ||
centriole | ||
perinuclear region of cytoplasm | ||
midbody | ||
mitochondrion |
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: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 |
---|---|---|---|
100189919 | PONAB14186 | ||
112928407 | VULVU23070 | ||
123784455 | URSAM25784 | ||
101682580 | MUSPF03289 | ||
101099513 | FELCA34732 | ||
118885507 | BALMU16631 | ||
100660519 | LOXAF03471 | ||
100125964 | PIGXX27798 | ||
102181151 | CAPHI08967 | ||
101113169 | SHEEP05367 |
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Last updated: August 19, 2024