decreased digestive secretion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the production and/or release of a physiologically active substance (usually but not exclusively in liquid form) from a cell or a gland of the digestive system (Mammalian Phenotype Ontology, MP_0000505)
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12 gene mutations causing the decreased digestive secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHRM3 cholinergic receptor, muscarinic 3
CHRM5 cholinergic receptor, muscarinic 5
CPE carboxypeptidase E
FOXQ1 forkhead box Q1
HRH2 histamine receptor H2
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
MUC1 mucin 1, cell surface associated
NOS2 nitric oxide synthase 2, inducible
PRKG2 protein kinase, cGMP-dependent, type II
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
SLC26A9 solute carrier family 26 (anion exchanger), member 9
SYTL2 synaptotagmin-like 2