abnormal digestive secretion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly 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_0000501)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000501
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32 gene mutations causing the abnormal digestive secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP4A ATPase, H+/K+ exchanging, alpha polypeptide
CHRM3 cholinergic receptor, muscarinic 3
CHRM5 cholinergic receptor, muscarinic 5
CPE carboxypeptidase E
EZR ezrin
FOXL1 forkhead box L1
FOXQ1 forkhead box Q1
GAST gastrin
GPR39 G protein-coupled receptor 39
GUCA2B guanylate cyclase activator 2B (uroguanylin)
HOXA5 homeobox A5
HRH2 histamine receptor H2
IL18 interleukin 18
JCHAIN joining chain of multimeric IgA and IgM
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LASP1 LIM and SH3 protein 1
MUC1 mucin 1, cell surface associated
NOS2 nitric oxide synthase 2, inducible
P2RY4 pyrimidinergic receptor P2Y, G-protein coupled, 4
PIGR polymeric immunoglobulin receptor
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
SLC4A2 solute carrier family 4 (anion exchanger), member 2
SLC9A2 solute carrier family 9, subfamily A (NHE2, cation proton antiporter 2), member 2
SLC9A4 solute carrier family 9, subfamily A (NHE4, cation proton antiporter 4), member 4
SST somatostatin
SYTL2 synaptotagmin-like 2
TFF2 trefoil factor 2
TP73 tumor protein p73
TRIM50 tripartite motif containing 50