Hearing Loss, Sensorineural Gene Set

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

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

Symbol Name
APOE apolipoprotein E
AQP4 aquaporin 4
AQP5 aquaporin 5
ATP6V1B1 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
CAV1 caveolin 1, caveolae protein, 22kDa
CFH complement factor H
CLDN23 claudin 23
COL2A1 collagen, type II, alpha 1
COL9A3 collagen, type IX, alpha 3
CYBA cytochrome b-245, alpha polypeptide
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
DEFA3 defensin, alpha 3, neutrophil-specific
DFNB13 deafness, autosomal recessive 13
EDN1 endothelin 1
ESR1 estrogen receptor 1
ESRRB estrogen-related receptor beta
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
FOXI1 forkhead box I1
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB4 gap junction protein, beta 4, 30.3kDa
GJB5 gap junction protein, beta 5, 31.1kDa
GJB6 gap junction protein, beta 6, 30kDa
GJC3 gap junction protein, gamma 3, 30.2kDa
GPX1 glutathione peroxidase 1
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
HBB hemoglobin, beta
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HSPA1A heat shock 70kDa protein 1A
IFNG interferon, gamma
IL10 interleukin 10
IL1B interleukin 1, beta
IL4R interleukin 4 receptor
IL5 interleukin 5
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
LOR loricrin
LRTOMT leucine rich transmembrane and O-methyltransferase domain containing
LTA lymphotoxin alpha
MBL2 mannose-binding lectin (protein C) 2, soluble
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
MRPS18CP2 mitochondrial ribosomal protein S18C pseudogene 2
MT-CYB cytochrome b
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-TL1 tRNA
MT-TS1 tRNA
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTNR1B melatonin receptor 1B
MTO1 mitochondrial tRNA translation optimization 1
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MYO1C myosin IC
MYO1F myosin IF
MYO7A myosin VIIA
NOS1 nitric oxide synthase 1 (neuronal)
NOS2 nitric oxide synthase 2, inducible
NOS3 nitric oxide synthase 3 (endothelial cell)
OTOF otoferlin
PON1 paraoxonase 1
PON2 paraoxonase 2
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC26A5 solute carrier family 26 (anion exchanger), member 5
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SOD2 superoxide dismutase 2, mitochondrial
TECTA tectorin alpha
TLR10 toll-like receptor 10
TLR2 toll-like receptor 2
TLR3 toll-like receptor 3
TLR4 toll-like receptor 4
TLR7 toll-like receptor 7
TLR8 toll-like receptor 8
TLR9 toll-like receptor 9
TNF tumor necrosis factor
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B
TRL-TAG1-1 transfer RNA-Leu (TAG) 1-1
TRMU tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase
TRNL
TRS-AGA2-4 transfer RNA-Ser (AGA) 2-4
UBQLN1 ubiquilin 1
USH2A Usher syndrome 2A (autosomal recessive, mild)
VEGFA vascular endothelial growth factor A
WFS1 Wolfram syndrome 1 (wolframin)
WRN Werner syndrome, RecQ helicase-like