abnormal nerve conduction Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005403
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47 gene mutations causing the abnormal nerve conduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CANX calnexin
CCR10 chemokine (C-C motif) receptor 10
CD86 CD86 molecule
CLCN2 chloride channel, voltage-sensitive 2
CNTNAP1 contactin associated protein 1
EBF2 early B-cell factor 2
EGR2 early growth response 2
ERBB2IP erbb2 interacting protein
ETV1 ets variant 1
FGD4 FYVE, RhoGEF and PH domain containing 4
FIG4 FIG4 phosphoinositide 5-phosphatase
GARS glycyl-tRNA synthetase
GBX1 gastrulation brain homeobox 1
GJB1 gap junction protein, beta 1, 32kDa
GNPAT glyceronephosphate O-acyltransferase
LAMA2 laminin, alpha 2
LEP leptin
LEPR leptin receptor
LPIN1 lipin 1
LRSAM1 leucine rich repeat and sterile alpha motif containing 1
MAP1B microtubule-associated protein 1B
MPZ myelin protein zero
MTMR2 myotubularin related protein 2
NALCN sodium leak channel, non selective
NDRG1 N-myc downstream regulated 1
NFASC neurofascin
NKX6-2 NK6 homeobox 2
NRCAM neuronal cell adhesion molecule
NRG1 neuregulin 1
PARL presenilin associated, rhomboid-like
PARP10 poly (ADP-ribose) polymerase family, member 10
PHYH phytanoyl-CoA 2-hydroxylase
PLEC plectin
PLP1 proteolipid protein 1
PMP22 peripheral myelin protein 22
PRX periaxin
SBF2 SET binding factor 2
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SH3TC2 SH3 domain and tetratricopeptide repeats 2
SHC1 SHC (Src homology 2 domain containing) transforming protein 1
SLC1A6 solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6
SLC5A3 solute carrier family 5 (sodium/myo-inositol cotransporter), member 3
STMN1 stathmin 1
TNR tenascin R
UGT8 UDP glycosyltransferase 8