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: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 | |
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 |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
105999295 | DIPOR05866 | ||
100752856 | CRIGR22589 | ||
113830659 | CRIGR22589 | ||
13806 | MGI:95393 | MOUSE24213 | |
433182 | MGI:3648653 | MOUSE24213 | |
24333 | RGD:2553 | RATNO33198 | |
688509 | RGD:1587670 | ||
100306968 | CAVPO11937 | ||
101579254 | OCTDE22695 | ||
101875019 | MELUD17592 |
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Last updated: August 19, 2024