abnormal parasympathetic ganglion morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the ganglia of the parasympathetic nervous system, including the ciliary, pterygopalatine, submandibular, and otic ganglia in the cranial region and intrinsic (terminal) ganglia associated with target organs in the thorax and abdomen (Mammalian Phenotype Ontology, MP_0001034)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001034
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Genes

9 gene mutations causing the abnormal parasympathetic ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASCL1 achaete-scute family bHLH transcription factor 1
GFRA1 GDNF family receptor alpha 1
GFRA2 GDNF family receptor alpha 2
NEUROG2 neurogenin 2
NRTN neurturin
OTX2 orthodenticle homeobox 2
PHOX2A paired-like homeobox 2a
PHOX2B paired-like homeobox 2b
RET ret proto-oncogene