intestinal hypoperistalsis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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10 gene mutations causing the intestinal hypoperistalsis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DLX2 distal-less homeobox 2
GDNF glial cell derived neurotrophic factor
GFRA1 GDNF family receptor alpha 1
GFRA2 GDNF family receptor alpha 2
GUCY1B3 guanylate cyclase 1, soluble, beta 3
MYH11 myosin, heavy chain 11, smooth muscle
NRTN neurturin
NTSR1 neurotensin receptor 1 (high affinity)
RET ret proto-oncogene
SMTN smoothelin