abnormal gastric gland morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of any of the branched tubular glands in the mucosa of the fundus and body of the stomach that contain parietal cells that secrete hydrochloric acid and zymogenic cells that produce pepsin (Mammalian Phenotype Ontology, MP_0003892)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003892
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27 gene mutations causing the abnormal gastric gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGR2 anterior gradient 2
ATP4A ATPase, H+/K+ exchanging, alpha polypeptide
ATP4B ATPase, H+/K+ exchanging, beta polypeptide
BHLHA15 basic helix-loop-helix family, member a15
CA9 carbonic anhydrase IX
CCKBR cholecystokinin B receptor
CLDN18 claudin 18
EZR ezrin
FGF10 fibroblast growth factor 10
FOXL1 forkhead box L1
GAST gastrin
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
OCLN occludin
PDX1 pancreatic and duodenal homeobox 1
RUNX3 runt-related transcription factor 3
SEC23B Sec23 homolog B (S. cerevisiae)
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
SMAD1 SMAD family member 1
SST somatostatin
TRIM50 tripartite motif containing 50