abnormal nodose ganglion morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the large group of sensory neuron cell bodies, anterior to the jugular vein, associated with the vagus nerve (tenth cranial nerve) (Mammalian Phenotype Ontology, MP_0001087)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001087
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Genes

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

Symbol Name
BDNF brain-derived neurotrophic factor
CHRD chordin
ERBB3 erb-b2 receptor tyrosine kinase 3
GFRA1 GDNF family receptor alpha 1
NRG1 neuregulin 1
NTF3 neurotrophin 3
NTF4 neurotrophin 4
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
PHOX2A paired-like homeobox 2a
PHOX2B paired-like homeobox 2b
SOX10 SRY (sex determining region Y)-box 10