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 |
---|---|---|
cell surface | ||
plasma membrane | ||
extracellular space | ||
nuclear outer membrane | ||
membrane |
GO Term | Evidence Code | PMID |
---|---|---|
protein binding | ||
cadherin binding | ||
RNA binding | ||
transcription corepressor activity | ||
phosphopyruvate hydratase activity |
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 |
---|---|---|---|
174423 | WB:WBGene00011884 | ||
33351 | FB:FBgn0000579 | ||
100177203 | CIOIN10292 | ||
103184183 | CALMI29259 | ||
102350577 | LATCH20254 | ||
334116 | ZFIN:ZDB-GENE-030131-6048 | DANRE25120 | |
393668 | ZFIN:ZDB-GENE-040426-1651 | ||
103038459 | ASTMX05247 | ||
100304706 | ICTPU07902 | ||
113586220 | ELEEL36772 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 19, 2024