abnormal circulating gastrin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalous concentration in the blood of polypeptide hormones secreted by the pyloric-antral mucous lining of the stomach that induces the secretion of gastric juice by the parietal cells of the gastric glands; they also occur in the central nervous system where they are presumed to be neurotransmitters (Mammalian Phenotype Ontology, MP_0004730)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004730
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10 gene mutations causing the abnormal circulating gastrin level 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
CPE carboxypeptidase E
HRH2 histamine receptor H2
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
SST somatostatin