abnormal stomach epithelium morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the epithelial layer of the stomach (Mammalian Phenotype Ontology, MP_0000471)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000471
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Genes

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

Symbol Name
A4GNT alpha-1,4-N-acetylglucosaminyltransferase
AGR2 anterior gradient 2
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
BHLHA15 basic helix-loop-helix family, member a15
CA2 carbonic anhydrase II
CA9 carbonic anhydrase IX
ERBB3 erb-b2 receptor tyrosine kinase 3
FOXL1 forkhead box L1
GDF11 growth differentiation factor 11
GRHL3 grainyhead-like 3 (Drosophila)
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
KITLG KIT ligand
KRT4 keratin 4, type II
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
OCLN occludin
RUNX3 runt-related transcription factor 3
SEC23B Sec23 homolog B (S. cerevisiae)
SHARPIN SHANK-associated RH domain interactor
SHH sonic hedgehog
SLC26A9 solute carrier family 26 (anion exchanger), member 9
SLC4A2 solute carrier family 4 (anion exchanger), member 2
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
THBS1 thrombospondin 1
TP63 tumor protein p63
TTC7A tetratricopeptide repeat domain 7A
VSIG1 V-set and immunoglobulin domain containing 1