abnormal enteric neuron morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the neurons that innervate the esophagus, stomach, small and large bowel (Mammalian Phenotype Ontology, MP_0001046)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001046
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Genes

18 gene mutations causing the abnormal enteric neuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARTN artemin
ASCL1 achaete-scute family bHLH transcription factor 1
ECE1 endothelin converting enzyme 1
EDN3 endothelin 3
EDNRB endothelin receptor type B
GDNF glial cell derived neurotrophic factor
GFRA1 GDNF family receptor alpha 1
HLX H2.0-like homeobox
IHH indian hedgehog
KIF26A kinesin family member 26A
NRTN neurturin
RET ret proto-oncogene
SALL4 spalt-like transcription factor 4
SHH sonic hedgehog
SOX10 SRY (sex determining region Y)-box 10
SPRY2 sprouty homolog 2 (Drosophila)
TLX2 T-cell leukemia homeobox 2
ZIC2 Zic family member 2