abnormal sympathetic ganglion morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the ganglia of the sympathetic nervous system including the paravertebral and the prevertebral ganglia, which include the sympathetic chain ganglia, the superior, middle, and inferior cervical ganglia, and the aorticorenal, celiac, and stellate ganglia (Mammalian Phenotype Ontology, MP_0001008)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001008
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Genes

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

Symbol Name
ARTN artemin
ASCL1 achaete-scute family bHLH transcription factor 1
BAX BCL2-associated X protein
BCL2 B-cell CLL/lymphoma 2
CREB1 cAMP responsive element binding protein 1
DLL3 delta-like 3 (Drosophila)
DUSP1 dual specificity phosphatase 1
EGLN3 egl-9 family hypoxia-inducible factor 3
ERBB2 erb-b2 receptor tyrosine kinase 2
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
NF1 neurofibromin 1
NGF nerve growth factor (beta polypeptide)
NRG1 neuregulin 1
NTF3 neurotrophin 3
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PDS5B PDS5 cohesin associated factor B
PHOX2A paired-like homeobox 2a
PHOX2B paired-like homeobox 2b
RET ret proto-oncogene
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SOX10 SRY (sex determining region Y)-box 10
SOX11 SRY (sex determining region Y)-box 11