increased bile salt level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased concentration of the steroid salts derived from cholesterol in the liver, produced as bile acids and secreted in the biliary system as bile salts; these play an important role in the digestion and absorption of fats (Mammalian Phenotype Ontology, MP_0004789)
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12 gene mutations causing the increased bile salt level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11
FABP6 fatty acid binding protein 6, ileal
GCGR glucagon receptor
IFT88 intraflagellar transport 88
MBOAT4 membrane bound O-acyltransferase domain containing 4
MIR122 microRNA 122
NR0B2 nuclear receptor subfamily 0, group B, member 2
NR1H4 nuclear receptor subfamily 1, group H, member 4
PCSK9 proprotein convertase subtilisin/kexin type 9
SIK3 SIK family kinase 3
SLC13A1 solute carrier family 13 (sodium/sulfate symporter), member 1
STARD10 StAR-related lipid transfer (START) domain containing 10