Hearing Disorders Gene Set
Genes
11 genes associated with the Hearing Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
FABP2
|
fatty acid binding protein 2, intestinal
|
|
GJB2
|
gap junction protein, beta 2, 26kDa
|
|
GSTM1
|
glutathione S-transferase mu 1
|
|
GSTT1
|
glutathione S-transferase theta 1
|
|
LRP2
|
low density lipoprotein receptor-related protein 2
|
|
MT-TL1
|
tRNA
|
|
MYO7A
|
myosin VIIA
|
|
NAT2
|
N-acetyltransferase 2 (arylamine N-acetyltransferase)
|
|
SLC6A4
|
solute carrier family 6 (neurotransmitter transporter), member 4
|
|
UCP1
|
uncoupling protein 1 (mitochondrial, proton carrier)
|
|
UCP2
|
uncoupling protein 2 (mitochondrial, proton carrier)
|
