abnormal vagus 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 vagus nerve (Mammalian Phenotype Ontology, MP_0001100)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001100
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Genes

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

Symbol Name
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
ARHGAP35 Rho GTPase activating protein 35
BDNF brain-derived neurotrophic factor
CHRD chordin
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
EGR2 early growth response 2
ERBB2 erb-b2 receptor tyrosine kinase 2
ERBB3 erb-b2 receptor tyrosine kinase 3
GFRA1 GDNF family receptor alpha 1
HOXA1 homeobox A1
MECOM MDS1 and EVI1 complex locus
NEUROG1 neurogenin 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)
SOX10 SRY (sex determining region Y)-box 10
TBX1 T-box 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)