fat malabsorption Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of the absorption of fat from the gastrointestinal tract. (Human Phenotype Ontology, HP_0002630)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002630
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Genes

21 genes associated with the fat malabsorption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11
AKR1D1 aldo-keto reductase family 1, member D1
AMACR alpha-methylacyl-CoA racemase
APOB apolipoprotein B
ATP8B1 ATPase, aminophospholipid transporter, class I, type 8B, member 1
BAAT bile acid CoA:amino acid N-acyltransferase
COX4I2 cytochrome c oxidase subunit IV isoform 2 (lung)
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
HSD3B7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7
LBR lamin B receptor
LIPA lipase A, lysosomal acid, cholesterol esterase
MTTP microsomal triglyceride transfer protein
PEX12 peroxisomal biogenesis factor 12
PNLIP pancreatic lipase
PRSS1 protease, serine, 1 (trypsin 1)
SAR1B secretion associated, Ras related GTPase 1B
SBDS Shwachman-Bodian-Diamond syndrome
SLC10A2 solute carrier family 10 (sodium/bile acid cotransporter), member 2
SPINK1 serine peptidase inhibitor, Kazal type 1
TJP2 tight junction protein 2