abnormal gastrointestinal motility Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the propulsive movements of the digestive system, resulting in the transit of the contents along the gastrointestinal tract (Mammalian Phenotype Ontology, MP_0011082)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011082
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Genes

39 gene mutations causing the abnormal gastrointestinal motility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AEBP2 AE binding protein 2
AGR2 anterior gradient 2
APC adenomatous polyposis coli
CCKAR cholecystokinin A receptor
CCKBR cholecystokinin B receptor
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
DLX2 distal-less homeobox 2
DRD2 dopamine receptor D2
EDNRB endothelin receptor type B
FFAR3 free fatty acid receptor 3
GDNF glial cell derived neurotrophic factor
GFRA1 GDNF family receptor alpha 1
GFRA2 GDNF family receptor alpha 2
GPR39 G protein-coupled receptor 39
GUCY1B3 guanylate cyclase 1, soluble, beta 3
HMOX2 heme oxygenase 2
HOXA13 homeobox A13
KIF26A kinesin family member 26A
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
MRVI1 murine retrovirus integration site 1 homolog
MYH11 myosin, heavy chain 11, smooth muscle
NKX2-3 NK2 homeobox 3
NPR2 natriuretic peptide receptor 2
NRTN neurturin
NTSR1 neurotensin receptor 1 (high affinity)
OPRM1 opioid receptor, mu 1
PRKG1 protein kinase, cGMP-dependent, type I
PSAP prosaposin
RET ret proto-oncogene
RFX6 regulatory factor X, 6
SALL1 spalt-like transcription factor 1
SLC18A2 solute carrier family 18 (vesicular monoamine transporter), member 2
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
SLIT3 slit homolog 3 (Drosophila)
SMAD3 SMAD family member 3
SMTN smoothelin
SPRY2 sprouty homolog 2 (Drosophila)
STK11 serine/threonine kinase 11
VIPR1 vasoactive intestinal peptide receptor 1