hypoalphalipoproteinemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An decreased concentration of high-density lipoprotein cholesterol in the blood. (Human Phenotype Ontology, HP_0003233)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003233
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Genes

10 genes associated with the hypoalphalipoproteinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ALMS1 Alstrom syndrome protein 1
APOA1 apolipoprotein A-I
APOA5 apolipoprotein A-V
LCAT lecithin-cholesterol acyltransferase
LMNA lamin A/C
PPARG peroxisome proliferator-activated receptor gamma
PPP1R3A protein phosphatase 1, regulatory subunit 3A
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13
SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal