increased intestinal cholesterol absorption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description augmented ability of the body to take up cholesterol into the blood by absorption from the small intestine (Mammalian Phenotype Ontology, MP_0002646)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002646
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Genes

3 gene mutations causing the increased intestinal cholesterol absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
CCKAR cholecystokinin A receptor
NR0B2 nuclear receptor subfamily 0, group B, member 2