Hearing Loss, Noise-Induced Gene Set

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

37 genes associated with the Hearing Loss, Noise-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
CAT catalase
CDH23 cadherin-related 23
CLCNKB chloride channel, voltage-sensitive Kb
DFNB13 deafness, autosomal recessive 13
DNMT1 DNA (cytosine-5-)-methyltransferase 1
GJB1 gap junction protein, beta 1, 32kDa
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB4 gap junction protein, beta 4, 30.3kDa
GJB6 gap junction protein, beta 6, 30kDa
GPX1 glutathione peroxidase 1
GRHL2 grainyhead-like 2 (Drosophila)
GSTM1 glutathione S-transferase mu 1
GSTP1 glutathione S-transferase pi 1
GSTT1 glutathione S-transferase theta 1
HSPA1A heat shock 70kDa protein 1A
HSPA1B heat shock 70kDa protein 1B
HSPA1L heat shock 70kDa protein 1-like
HSPA2 heat shock 70kDa protein 2
IL1B interleukin 1, beta
IL4R interleukin 4 receptor
IL6 interleukin 6
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4
MT-TS1 tRNA
OGG1 8-oxoguanine DNA glycosylase
PCDH15 protocadherin-related 15
PON1 paraoxonase 1
PON2 paraoxonase 2
RNR1 RNA, ribosomal cluster 1
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SOD1 superoxide dismutase 1, soluble
SOD2 superoxide dismutase 2, mitochondrial
WFS1 Wolfram syndrome 1 (wolframin)