UniProt | Protein Name |
---|---|
A0A0A0MRF5 |
|
Q8IXJ6 |
|
GO Term | Evidence Code | PMID |
---|---|---|
regulation of myelination | ||
regulation of exit from mitosis | ||
mitotic nuclear membrane reassembly | ||
cellular lipid catabolic process | ||
negative regulation of transcription by RNA polymerase II |
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: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 |
---|---|---|---|
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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Last updated: August 19, 2024