cholelithiasis Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). (Experimental Factor Ontology, EFO_0004799)
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Genes

10 genes associated with the disease cholelithiasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
ABCB4	ATP-binding cassette, sub-family B (MDR/TAP), member 4
APOB	apolipoprotein B
APOE	apolipoprotein E
CCKAR	cholecystokinin A receptor
CETP	cholesteryl ester transfer protein, plasma
CYP7A1	cytochrome P450, family 7, subfamily A, polypeptide 1
HBB	hemoglobin, beta
LDLR	low density lipoprotein receptor
MICA	MHC class I polypeptide-related sequence A
UGT1A1	UDP glucuronosyltransferase 1 family, polypeptide A1