abnormal parasympathetic nervous system physiology Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	any functional 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_0006277)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006277
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Genes

7 gene mutations causing the abnormal parasympathetic nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
DBX1	developing brain homeobox 1
KDM6B	lysine (K)-specific demethylase 6B
NDN	necdin, melanoma antigen (MAGE) family member
NDUFS4	NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
NHLH1	nescient helix loop helix 1
ROBO3	roundabout, axon guidance receptor, homolog 3 (Drosophila)
SLC17A6	solute carrier family 17 (vesicular glutamate transporter), member 6