abnormal motor nerve conduction velocity Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0040131
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Genes

30 genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AARS alanyl-tRNA synthetase
ATXN1 ataxin 1
CCT5 chaperonin containing TCP1, subunit 5 (epsilon)
CTDP1 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
DCAF8 DDB1 and CUL4 associated factor 8
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
EGR2 early growth response 2
FAM126A family with sequence similarity 126, member A
FGD4 FYVE, RhoGEF and PH domain containing 4
GDAP1 ganglioside induced differentiation associated protein 1
GJB1 gap junction protein, beta 1, 32kDa
GJC2 gap junction protein, gamma 2, 47kDa
HK1 hexokinase 1
HSPB1 heat shock 27kDa protein 1
KIF1B kinesin family member 1B
LITAF lipopolysaccharide-induced TNF factor
LMNA lamin A/C
MED25 mediator complex subunit 25
MFN2 mitofusin 2
MPZ myelin protein zero
MTMR2 myotubularin related protein 2
NALCN sodium leak channel, non selective
NEFL neurofilament, light polypeptide
PMP22 peripheral myelin protein 22
PRX periaxin
RAB7A RAB7A, member RAS oncogene family
SBF2 SET binding factor 2
SETX senataxin
SH3TC2 SH3 domain and tetratricopeptide repeats 2
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6