stomach mucosa hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description overdevelopment or increased size, usually due to an increase in the number of cells, of the mucous layer of the stomach wall which contains the gastric pits and glands, and consists of epithelium, lamina propria, and the muscularis mucosae (Mammalian Phenotype Ontology, MP_0010799)
External Link
Similar Terms
Downloads & Tools


11 gene mutations causing the stomach mucosa hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGR2 anterior gradient 2
ATP4B ATPase, H+/K+ exchanging, beta polypeptide
FOXL1 forkhead box L1
GPX7 glutathione peroxidase 7
HRH2 histamine receptor H2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KEAP1 kelch-like ECH-associated protein 1
NEUROG3 neurogenin 3
OCLN occludin
RUNX3 runt-related transcription factor 3
TFF1 trefoil factor 1