abnormal chief cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004140
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13 gene mutations causing the abnormal chief cell 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
BHLHA15 basic helix-loop-helix family, member a15
CLDN18 claudin 18
FGF10 fibroblast growth factor 10
FOXL1 forkhead box L1
GAST gastrin
HRH2 histamine receptor H2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
OCLN occludin
RUNX3 runt-related transcription factor 3
SLC4A2 solute carrier family 4 (anion exchanger), member 2
SLC9A4 solute carrier family 9, subfamily A (NHE4, cation proton antiporter 4), member 4