Hearing Disorders Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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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)