abnormal intestinal 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 cells present throughout the mucosa of the intestinal tract (Mammalian Phenotype Ontology, MP_0010802)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010802
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5 gene mutations causing the abnormal intestinal enteroendocrine cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CBFA2T2 core-binding factor, runt domain, alpha subunit 2; translocated to, 2
MYC v-myc avian myelocytomatosis viral oncogene homolog
NEUROD1 neuronal differentiation 1
SAV1 salvador family WW domain containing protein 1
TCF7L2 transcription factor 7-like 2 (T-cell specific, HMG-box)