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 |
---|---|---|---|
101977591 | ICTTR03058 | ||
118299053 | SCOMX22779 | ||
102417115 | MYOLU10190 | ||
117034493 | RHIFE01674 | ||
103234644 | CHLSB15725 | ||
114603233 | PODMU32203 | ||
107567264 | SINGR92626 | ||
116822396 | CHEAB08796 | ||
105300229 | PTEVA02847 | ||
115052846 | ECHNA07653 |
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Last updated: August 19, 2024