abnormality of the level of lipoprotein cholesterol Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal increase or decrease in the level of lipoprotein cholesterol in the blood. (Human Phenotype Ontology, HP_0010979)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010979
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22 genes associated with the abnormality of the level of lipoprotein cholesterol 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
ANGPTL3 angiopoietin-like 3
APOA1 apolipoprotein A-I
APOA5 apolipoprotein A-V
APOB apolipoprotein B
APOC3 apolipoprotein C-III
CCT5 chaperonin containing TCP1, subunit 5 (epsilon)
CETP cholesteryl ester transfer protein, plasma
LCAT lecithin-cholesterol acyltransferase
LDLRAP1 low density lipoprotein receptor adaptor protein 1
LMNA lamin A/C
LPL lipoprotein lipase
MTTP microsomal triglyceride transfer protein
PANK2 pantothenate kinase 2
PPARG peroxisome proliferator-activated receptor gamma
PPP1R3A protein phosphatase 1, regulatory subunit 3A
SAR1B secretion associated, Ras related GTPase 1B
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13
SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal
TTPA tocopherol (alpha) transfer protein
UBR1 ubiquitin protein ligase E3 component n-recognin 1