UniProt | Protein Name |
---|---|
A0A0A0MRF5 |
|
Q8IXJ6 |
|
GO Term | Evidence Code | PMID |
---|---|---|
negative regulation of satellite cell differentiation | ||
peptidyl-lysine deacetylation | ||
substantia nigra development | ||
post-translational protein modification | ||
rDNA heterochromatin formation |
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: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 |
---|---|---|---|
42414 | FB:FBgn0038788 | ||
100185251 | CIOIN12353 | ||
322309 | ZFIN:ZDB-GENE-030131-1028 | DANRE08771 | |
103038996 | ASTMX16188 | ||
128628623 | ICTPU15164 | ||
113584652 | ELEEL34062 | ||
115163165 | SALTR98772 | ||
115561108 | GADMO18756 | ||
100690476 | ORENI17756 | ||
115570409 | SPAAU16743 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024