abnormal ventral spinal root morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the anterior bundle of nerves emerging from the spinal cord to join with the posterior/dorsal nerve bundle at each spinal cord segment to form one of the 31 paired peripheral nerves (Mammalian Phenotype Ontology, MP_0003993)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003993
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Genes

18 gene mutations causing the abnormal ventral spinal root morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTPBP1 ATP/GTP binding protein 1
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
CD86 CD86 molecule
CUX2 cut-like homeobox 2
DOCK3 dedicator of cytokinesis 3
ERBB2 erb-b2 receptor tyrosine kinase 2
ERBB3 erb-b2 receptor tyrosine kinase 3
ETV1 ets variant 1
GAN gigaxonin
LAMA4 laminin, alpha 4
NEFH neurofilament, heavy polypeptide
NEFL neurofilament, light polypeptide
NEFM neurofilament, medium polypeptide
NRG1 neuregulin 1
PSAP prosaposin
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SOX10 SRY (sex determining region Y)-box 10