absent petrosal ganglion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the lower group of sensory neuron cell bodies associated with the glossopharyngeal nerve (Mammalian Phenotype Ontology, MP_0001086)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001086
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2 gene mutations causing the absent petrosal ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHRD chordin
EYA1 EYA transcriptional coactivator and phosphatase 1