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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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