UniProt | Protein Name |
---|---|
P06733 |
|
A0A024R4F1 |
|
GO Term | Evidence Code | PMID |
---|---|---|
positive regulation of plasminogen activation | ||
negative regulation of hypoxia-induced intrinsic apoptotic signaling pathway | ||
negative regulation of transcription, DNA-templated | ||
negative regulation of DNA-templated transcription | ||
negative regulation of cell growth |
GO Term | Evidence Code | PMID |
---|---|---|
magnesium ion binding | ||
protein homodimerization activity | ||
DNA-binding transcription repressor activity, RNA polymerase II-specific | ||
GTPase binding | ||
transcription corepressor binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
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 | |
DOID:0110300 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1A | |
DOID:0110301 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1B | |
DOID:0110302 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1C | |
DOID:0110303 | autosomal dominant limb-girdle muscular dystrophy type 1H | |
DOID:0110304 | autosomal dominant limb-girdle muscular dystrophy type 2 |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100194865 | SALSA40808 | ||
106566383 | SALSA26620 | ||
115165310 | SALTR86418 | ||
115168704 | SALTR86418 | ||
115553474 | GADMO28224 | ||
101163325 | ORYLA15651 | ||
100701182 | ORENI37654 | ||
115584809 | SPAAU50469 | ||
379079 | Xenbase:XB-GENE-483504 | ||
380298 | Xenbase:XB-GENE-6256554 |
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Last updated: August 19, 2024