abnormal superior cervical ganglion morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the group of neurons that is the largest of the sympathetic trunk; normally lies at the base of the skull and innervates the head and neck (Mammalian Phenotype Ontology, MP_0001011)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001011
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Genes

19 gene mutations causing the abnormal superior cervical ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARTN artemin
BAX BCL2-associated X protein
BCL2 B-cell CLL/lymphoma 2
CREB1 cAMP responsive element binding protein 1
DUSP1 dual specificity phosphatase 1
EGLN3 egl-9 family hypoxia-inducible factor 3
ERBB3 erb-b2 receptor tyrosine kinase 3
FFAR3 free fatty acid receptor 3
GDNF glial cell derived neurotrophic factor
GFRA3 GDNF family receptor alpha 3
HRK harakiri, BCL2 interacting protein
MAGED1 melanoma antigen family D1
NGF nerve growth factor (beta polypeptide)
NTF3 neurotrophin 3
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PDS5B PDS5 cohesin associated factor B
PHOX2A paired-like homeobox 2a
RET ret proto-oncogene
SOX10 SRY (sex determining region Y)-box 10