abnormal intestinal absorption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the quantity or rate of any nutrient taken up from the contents of the intestine (Mammalian Phenotype Ontology, MP_0001666)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001666
Similar Terms
Downloads & Tools

Genes

47 gene mutations causing the abnormal intestinal 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
DRD2 dopamine receptor D2
EGFR epidermal growth factor receptor
FCER2 Fc fragment of IgE, low affinity II, receptor for (CD23)
FGFR2 fibroblast growth factor receptor 2
GCNT3 glucosaminyl (N-acetyl) transferase 3, mucin type
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
HSD3B7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7
KRT8 keratin 8, type II
MOGAT2 monoacylglycerol O-acyltransferase 2
MRAP2 melanocortin 2 receptor accessory protein 2
MUC1 mucin 1, cell surface associated
MUC2 mucin 2, oligomeric mucus/gel-forming
NPC1L1 NPC1-like 1
NR0B2 nuclear receptor subfamily 0, group B, member 2
PEX1 peroxisomal biogenesis factor 1
PHEX phosphate regulating endopeptidase homolog, X-linked
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
RAB8A RAB8A, member RAS oncogene family
RBP2 retinol binding protein 2, cellular
RSC1A1 regulatory solute carrier protein, family 1, member 1
SLC10A2 solute carrier family 10 (sodium/bile acid cotransporter), member 2
SLC15A1 solute carrier family 15 (oligopeptide transporter), member 1
SLC16A1 solute carrier family 16 (monocarboxylate transporter), member 1
SLC19A3 solute carrier family 19 (thiamine transporter), member 3
SLC23A1 solute carrier family 23 (ascorbic acid transporter), member 1
SLC2A8 solute carrier family 2 (facilitated glucose transporter), member 8
SLC30A7 solute carrier family 30 (zinc transporter), member 7
SLC34A3 solute carrier family 34 (type II sodium/phosphate cotransporter), member 3
SOAT2 sterol O-acyltransferase 2
TFRC transferrin receptor
TMPRSS6 transmembrane protease, serine 6
TREH trehalase (brush-border membrane glycoprotein)
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor