UniProt | Protein Name |
---|---|
P30613 |
|
GO Term | Evidence Code | PMID |
---|---|---|
response to ATP | ||
response to hypoxia | ||
pyruvate biosynthetic process | ||
phosphorylation |
|
|
response to cAMP |
GO Term | Evidence Code | PMID |
---|---|---|
cytosol | ||
cytoplasm | ||
pyruvate kinase complex |
|
|
extracellular exosome |
GO Term | Evidence Code | PMID |
---|---|---|
kinase activity | ||
magnesium ion binding | ||
potassium ion binding | ||
monosaccharide binding | ||
ATP binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:2373 | hereditary elliptocytosis | |
DOID:2491 | sensory peripheral neuropathy | |
DOID:2834 | acquired polycythemia | |
DOID:2838 | stress polycythemia | |
DOID:2839 | erythropoietin polycythemia | |
DOID:2848 | obsolete melancholia | |
DOID:2860 | hemoglobinopathy | |
DOID:2861 | congenital nonspherocytic hemolytic anemia | |
DOID:3121 | gallbladder cancer | |
DOID:3459 | breast carcinoma |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000007 | Autosomal recessive inheritance |
HP:0000952 | Jaundice |
HP:0000980 | Pallor |
HP:0001081 | Cholelithiasis |
HP:0001082 | Cholecystitis |
HP:0001511 | Intrauterine growth retardation |
HP:0001744 | Splenomegaly |
HP:0001789 | Hydrops fetalis |
HP:0001790 | Nonimmune hydrops fetalis |
Disease ID | Disease Name |
---|---|
OMIM:102900 |
|
ORPHA:766 |
|
OMIM:266200 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100355056 | RABIT03326 | ||
100755461 | CRIGR08927 | ||
18770 | MGI:97604 | MOUSE38518 | |
24651 | RGD:3336 | RATNO22779 | |
100716756 | CAVPO06444 | ||
101560835 | OCTDE06856 | ||
100022269 | MONDO12520 | ||
113885573 | BOBOX07266 | ||
100955995 | OTOGA07411 | ||
446067 | TAKRU46373 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024