abnormal stomach ph Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the function of the secretory and buffer systems of the stomach that control the relative acidity or alkalinity, as measured by the concentration of the hydrogen ion (Mammalian Phenotype Ontology, MP_0008004)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008004
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Genes

14 gene mutations causing the abnormal stomach ph phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP4A ATPase, H+/K+ exchanging, alpha polypeptide
ATP4B ATPase, H+/K+ exchanging, beta polypeptide
CCKBR cholecystokinin B receptor
GAST gastrin
HRH2 histamine receptor H2
IL6ST interleukin 6 signal transducer
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
MCOLN1 mucolipin 1
NKX6-3 NK6 homeobox 3
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
SLC26A9 solute carrier family 26 (anion exchanger), member 9
TRIM50 tripartite motif containing 50
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