abnormal petrosal ganglion morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the larger, lower group of sensory neuron cell bodies associated with the glossopharyngeal nerve (Mammalian Phenotype Ontology, MP_0001084)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001084
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Genes

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

Symbol Name
BDNF brain-derived neurotrophic factor
CHRD chordin
ERBB2 erb-b2 receptor tyrosine kinase 2
ERBB3 erb-b2 receptor tyrosine kinase 3
EYA1 EYA transcriptional coactivator and phosphatase 1
GFRA1 GDNF family receptor alpha 1
NEUROG2 neurogenin 2
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