abnormal geniculate ganglion morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the group of sensory neuron cell bodies associated with the facial nerve (seventh cranial nerve) (Mammalian Phenotype Ontology, MP_0001082)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001082
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16 gene mutations causing the abnormal geniculate ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BDNF brain-derived neurotrophic factor
CHRD chordin
EGR2 early growth response 2
ERBB2 erb-b2 receptor tyrosine kinase 2
ERBB4 erb-b2 receptor tyrosine kinase 4
EYA1 EYA transcriptional coactivator and phosphatase 1
HOXA1 homeobox A1
HOXB2 homeobox B2
NEUROG2 neurogenin 2
NTF3 neurotrophin 3
NTF4 neurotrophin 4
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PHOX2A paired-like homeobox 2a
PHOX2B paired-like homeobox 2b
POU4F1 POU class 4 homeobox 1
RDH10 retinol dehydrogenase 10 (all-trans)