decreased nerve conduction velocity Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A reduction in the speed at which electrical signals propagate along the axon of a neuron. (Human Phenotype Ontology, HP_0000762)
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26 gene mutations causing the decreased nerve conduction velocity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CANX calnexin
CCR10 chemokine (C-C motif) receptor 10
CD86 CD86 molecule
CNTNAP1 contactin associated protein 1
EBF2 early B-cell factor 2
EGR2 early growth response 2
ERBB2IP erbb2 interacting protein
FGD4 FYVE, RhoGEF and PH domain containing 4
FIG4 FIG4 phosphoinositide 5-phosphatase
GARS glycyl-tRNA synthetase
GNPAT glyceronephosphate O-acyltransferase
LAMA2 laminin, alpha 2
LEP leptin
LPIN1 lipin 1
LRSAM1 leucine rich repeat and sterile alpha motif containing 1
NDRG1 N-myc downstream regulated 1
NFASC neurofascin
NRCAM neuronal cell adhesion molecule
PARP10 poly (ADP-ribose) polymerase family, member 10
PHYH phytanoyl-CoA 2-hydroxylase
PLEC plectin
PMP22 peripheral myelin protein 22
PRX periaxin
SH3TC2 SH3 domain and tetratricopeptide repeats 2
TNR tenascin R