abnormal glucose tolerance Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal resistance to glucose, i.e., a reduction in the ability to maintain glucose levels in the blood stream within normal limits following oral or intravenous administration of glucose. (Human Phenotype Ontology, HP_0001952)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001952
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14 genes associated with the abnormal glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIP aryl hydrocarbon receptor interacting protein
APOE apolipoprotein E
ATM ATM serine/threonine kinase
CAV1 caveolin 1, caveolae protein, 22kDa
HFE hemochromatosis
HNF1B HNF1 homeobox B
IFT172 intraflagellar transport 172
LMNA lamin A/C
NSD1 nuclear receptor binding SET domain protein 1
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
POLG2 polymerase (DNA directed), gamma 2, accessory subunit
SLC5A1 solute carrier family 5 (sodium/glucose cotransporter), member 1
WFS1 Wolfram syndrome 1 (wolframin)
ZMPSTE24 zinc metallopeptidase STE24