Hypertrophic Neuropathy Of Infancy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1408174
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Genes

21 genes associated with the disease Hypertrophic Neuropathy Of Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
COX6A1 cytochrome c oxidase subunit VIa polypeptide 1
DHTKD1 dehydrogenase E1 and transketolase domain containing 1
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
EGR2 early growth response 2
FGD4 FYVE, RhoGEF and PH domain containing 4
FIG4 FIG4 phosphoinositide 5-phosphatase
GARS glycyl-tRNA synthetase
GDAP1 ganglioside induced differentiation associated protein 1
GJB1 gap junction protein, beta 1, 32kDa
KIF1B kinesin family member 1B
LMNA lamin A/C
LRSAM1 leucine rich repeat and sterile alpha motif containing 1
MFN2 mitofusin 2
MPZ myelin protein zero
MTMR2 myotubularin related protein 2
NDRG1 N-myc downstream regulated 1
NEFL neurofilament, light polypeptide
PMP22 peripheral myelin protein 22
SBF2 SET binding factor 2
SH3TC2 SH3 domain and tetratricopeptide repeats 2
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6