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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Genes

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