impaired gluconeogenesis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An impairment of gluconeogenesis. (Human Phenotype Ontology, HP_0005959)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005959
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Genes

3 genes associated with the impaired gluconeogenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PCK1 phosphoenolpyruvate carboxykinase 1 (soluble)
PCK2 phosphoenolpyruvate carboxykinase 2 (mitochondrial)
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5