abnormal esophageal epithelium morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the epithelial layer that lines the luminal space of the esophagus (Mammalian Phenotype Ontology, MP_0000468)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000468
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14 gene mutations causing the abnormal esophageal epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
EGFR epidermal growth factor receptor
FZD4 frizzled class receptor 4
ITGB4 integrin, beta 4
KDF1 keratinocyte differentiation factor 1
KEAP1 kelch-like ECH-associated protein 1
KRT4 keratin 4, type II
KRT5 keratin 5, type II
RAB25 RAB25, member RAS oncogene family
SHARPIN SHANK-associated RH domain interactor
SLC4A2 solute carrier family 4 (anion exchanger), member 2
SLC9A3 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
SOX2 SRY (sex determining region Y)-box 2
TP63 tumor protein p63