abnormal stomach glandular epithelium morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the gland-containing epithelial layer of the stomach (Mammalian Phenotype Ontology, MP_0000473)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000473
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Genes

17 gene mutations causing the abnormal stomach glandular epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGR2 anterior gradient 2
BHLHA15 basic helix-loop-helix family, member a15
FOXL1 forkhead box L1
HHIP hedgehog interacting protein
HNF1A HNF1 homeobox A
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KEAP1 kelch-like ECH-associated protein 1
OCLN occludin
SEC23B Sec23 homolog B (S. cerevisiae)
SHH sonic hedgehog
SLC26A9 solute carrier family 26 (anion exchanger), member 9
SLC9A1 solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
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
SMAD4 SMAD family member 4
SPDEF SAM pointed domain containing ETS transcription factor
VSIG1 V-set and immunoglobulin domain containing 1
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