abnormal intestinal lipid absorption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the ability of the body to take up lipids into the blood by absorption from the small intestine (Mammalian Phenotype Ontology, MP_0005342)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005342
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Genes

23 gene mutations causing the abnormal intestinal lipid absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ALPI alkaline phosphatase, intestinal
C3 complement component 3
CCKAR cholecystokinin A receptor
CD36 CD36 molecule (thrombospondin receptor)
CEL carboxyl ester lipase
CLOCK clock circadian regulator
CYP7A1 cytochrome P450, family 7, subfamily A, polypeptide 1
CYP8B1 cytochrome P450, family 8, subfamily B, polypeptide 1
HSD3B7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7
MOGAT2 monoacylglycerol O-acyltransferase 2
MUC1 mucin 1, cell surface associated
NPC1L1 NPC1-like 1
NR0B2 nuclear receptor subfamily 0, group B, member 2
PEX1 peroxisomal biogenesis factor 1
PITPNA phosphatidylinositol transfer protein, alpha
PLA2G1B phospholipase A2, group IB (pancreas)
PLAGL2 pleiomorphic adenoma gene-like 2
PNLIP pancreatic lipase
PNLIPRP2 pancreatic lipase-related protein 2
SLC10A2 solute carrier family 10 (sodium/bile acid cotransporter), member 2
SOAT2 sterol O-acyltransferase 2