abnormal enteroendocrine cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the various hormone- or neurotransmitter-secreting epithelial cells present throughout the mucosa of the digestive tract (Mammalian Phenotype Ontology, MP_0004141)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004141
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12 gene mutations causing the abnormal enteroendocrine 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
CBFA2T2 core-binding factor, runt domain, alpha subunit 2; translocated to, 2
CCKBR cholecystokinin B receptor
GFRA2 GDNF family receptor alpha 2
INSM1 insulinoma-associated 1
MYC v-myc avian myelocytomatosis viral oncogene homolog
NEUROD1 neuronal differentiation 1
NKX6-3 NK6 homeobox 3
PDX1 pancreatic and duodenal homeobox 1
SAV1 salvador family WW domain containing protein 1
TCF7L2 transcription factor 7-like 2 (T-cell specific, HMG-box)