abnormal parasympathetic system morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the part of the autonomic nervous system that innervates smooth muscle, cardiac muscle and glands and generally acts to conserve resources and restore homeostasis, often with effects reciprocal to the sympathetic nervous system (Mammalian Phenotype Ontology, MP_0001033)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001033
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11 gene mutations causing the abnormal parasympathetic system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASCL1 achaete-scute family bHLH transcription factor 1
DBX1 developing brain homeobox 1
GFRA1 GDNF family receptor alpha 1
GFRA2 GDNF family receptor alpha 2
KDM6B lysine (K)-specific demethylase 6B
NEUROG2 neurogenin 2
NRTN neurturin
OTX2 orthodenticle homeobox 2
PHOX2A paired-like homeobox 2a
PHOX2B paired-like homeobox 2b
RET ret proto-oncogene