Auditory Neuropathy Gene Set
Genes
20 genes associated with the disease Auditory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
AIFM1
|
apoptosis-inducing factor, mitochondrion-associated, 1
|
|
ATP1A3
|
ATPase, Na+/K+ transporting, alpha 3 polypeptide
|
|
BHLHE22
|
basic helix-loop-helix family, member e22
|
|
DFNB59
|
deafness, autosomal recessive 59
|
|
DIAPH3
|
diaphanous-related formin 3
|
|
GJB2
|
gap junction protein, beta 2, 26kDa
|
|
MPZ
|
myelin protein zero
|
|
MYO7A
|
myosin VIIA
|
|
OPA1
|
optic atrophy 1 (autosomal dominant)
|
|
OTOF
|
otoferlin
|
|
PCDH9
|
protocadherin 9
|
|
SLC26A4
|
solute carrier family 26 (anion exchanger), member 4
|
|
SLC52A2
|
solute carrier family 52 (riboflavin transporter), member 2
|
|
SLITRK6
|
SLIT and NTRK-like family, member 6
|
|
SPTBN4
|
spectrin, beta, non-erythrocytic 4
|
|
STRC
|
stereocilin
|
|
TIMM8A
|
translocase of inner mitochondrial membrane 8 homolog A (yeast)
|
|
TMEM126A
|
transmembrane protein 126A
|
|
TMPRSS3
|
transmembrane protease, serine 3
|
|
TWNK
|
twinkle mtDNA helicase
|
