abnormal glossopharyngeal ganglion morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the two groups of sensory neuron cell bodies associated with the ninth cranial nerve (Mammalian Phenotype Ontology, MP_0001096)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001096
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28 gene mutations causing the abnormal glossopharyngeal ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
BDNF brain-derived neurotrophic factor
CHRD chordin
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
DST dystonin
EGR2 early growth response 2
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
HOXA1 homeobox A1
LMX1A LIM homeobox transcription factor 1, alpha
MECOM MDS1 and EVI1 complex locus
NEUROG1 neurogenin 1
NEUROG2 neurogenin 2
NR2F1 nuclear receptor subfamily 2, group F, member 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
PTK7 protein tyrosine kinase 7 (inactive)
RDH10 retinol dehydrogenase 10 (all-trans)
TBX1 T-box 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
ZIC5 Zic family member 5