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 |
---|---|---|---|
100476305 | AILME13321 | ||
117800325 | AILME13321 | ||
101680330 | MUSPF06416 | ||
101093622 | FELCA18465 | ||
122226567 | PANLE10563 | ||
118895771 | BALMU22092 | ||
100668262 | LOXAF11427 | ||
100738870 | PIGXX28963 | ||
102175881 | CAPHI06839 | ||
100352426 | RABIT04267 |
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Last updated: August 19, 2024