hearing Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description The series of events required for an organism to receive an auditory stimulus, convert it to a molecular signal, and recognize and characterize the signal. Sonic stimuli are detected in the form of vibrations and are processed to form a sound. (Gene Ontology, GO_0007605)
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Genes

193 genes co-occuring with the biological term hearing in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ABHD12 abhydrolase domain containing 12
ACE angiotensin I converting enzyme
ACTG1 actin gamma 1
ADCY1 adenylate cyclase 1 (brain)
ADIPOQ adiponectin, C1Q and collagen domain containing
ANKH ANKH inorganic pyrophosphate transport regulator
ANOS1 anosmin 1
APOE apolipoprotein E
AQP4 aquaporin 4
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
ATP6V1B1 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
ATP8B1 ATPase, aminophospholipid transporter, class I, type 8B, member 1
BDP1 B double prime 1, subunit of RNA polymerase III transcription initiation factor IIIB
C2ORF71 chromosome 2 open reading frame 71
CABP2 calcium binding protein 2
CAT catalase
CCDC50 coiled-coil domain containing 50
CDH23 cadherin-related 23
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CEP250 centrosomal protein 250kDa
CFH complement factor H
CHD7 chromodomain helicase DNA binding protein 7
CLDN14 claudin 14
CLDN9 claudin 9
COCH cochlin
COL11A2 collagen, type XI, alpha 2
COL1A1 collagen, type I, alpha 1
COL2A1 collagen, type II, alpha 1
COL4A4 collagen, type IV, alpha 4
COL4A6 collagen, type IV, alpha 6
COL9A3 collagen, type IX, alpha 3
COMT catechol-O-methyltransferase
COX2
CTBP2 C-terminal binding protein 2
DFNA18 deafness, autosomal dominant 18
DFNA24 deafness, autosomal dominant 24
DFNA5 deafness, autosomal dominant 5
DFNA52 deafness, autosomal dominant 52
DFNA54 deafness, autosomal dominant 54
DFNB40 deafness, autosomal recessive 40
DFNB45 deafness, autosomal recessive 45
DFNB55 deafness, autosomal recessive 55
DFNB59 deafness, autosomal recessive 59
DFNY1 deafness, Y-linked 1
DNMT1 DNA (cytosine-5-)-methyltransferase 1
EDN1 endothelin 1
EPO erythropoietin
ESPN espin
ESRRB estrogen-related receptor beta
ESRRG estrogen-related receptor gamma
EYA4 EYA transcriptional coactivator and phosphatase 4
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
FABP2 fatty acid binding protein 2, intestinal
FGB fibrinogen beta chain
FGFR3 fibroblast growth factor receptor 3
FLG filaggrin
GATA3 GATA binding protein 3
GIPC3 GIPC PDZ domain containing family, member 3
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
GJC1 gap junction protein, gamma 1, 45kDa
GJC3 gap junction protein, gamma 3, 30.2kDa
GJD2 gap junction protein, delta 2, 36kDa
GPSM2 G-protein signaling modulator 2
GRHL2 grainyhead-like 2 (Drosophila)
GRM7 glutamate receptor, metabotropic 7
GRXCR1 glutaredoxin, cysteine rich 1
GRXCR2 glutaredoxin, cysteine rich 2
GSTM1 glutathione S-transferase mu 1
GSTP1 glutathione S-transferase pi 1
GSTT1 glutathione S-transferase theta 1
HARS2 histidyl-tRNA synthetase 2, mitochondrial
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HMX2 H6 family homeobox 2
HMX3 H6 family homeobox 3
HOXA2 homeobox A2
HOXB1 homeobox B1
HSPA1A heat shock 70kDa protein 1A
HSPA1B heat shock 70kDa protein 1B
HSPA1L heat shock 70kDa protein 1-like
HSPA4 heat shock 70kDa protein 4
IFNG interferon, gamma
IL1B interleukin 1, beta
IL6 interleukin 6
ILDR1 immunoglobulin-like domain containing receptor 1
IQGAP2 IQ motif containing GTPase activating protein 2
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
KARS lysyl-tRNA synthetase
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
LARS2 leucyl-tRNA synthetase 2, mitochondrial
LHFPL5 lipoma HMGIC fusion partner-like 5
LHX3 LIM homeobox 3
LOXHD1 lipoxygenase homology domains 1
LRTOMT leucine rich transmembrane and O-methyltransferase domain containing
MARVELD2 MARVEL domain containing 2
MBL2 mannose-binding lectin (protein C) 2, soluble
MBP myelin basic protein
MCHR1 melanin-concentrating hormone receptor 1
MICA MHC class I polypeptide-related sequence A
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
MIR183 microRNA 183
MT-ATP6 ATP synthase F0 subunit 6
MT-ND4 NADH dehydrogenase, subunit 4 (complex I)
MT-TS1 tRNA
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MYH14 myosin, heavy chain 14, non-muscle
MYH9 myosin, heavy chain 9, non-muscle
MYO15A myosin XVA
MYO1A myosin IA
MYO1C myosin IC
MYO1F myosin IF
MYO3A myosin IIIA
MYO6 myosin VI
MYO7A myosin VIIA
NAT2 N-acetyltransferase 2 (arylamine N-acetyltransferase)
ND1
NEUROG1 neurogenin 1
NF2 neurofibromin 2 (merlin)
NLRP3 NLR family, pyrin domain containing 3
NOG noggin
NOS1 nitric oxide synthase 1 (neuronal)
NOS2 nitric oxide synthase 2, inducible
NOS3 nitric oxide synthase 3 (endothelial cell)
OPA1 optic atrophy 1 (autosomal dominant)
OTOA otoancorin
OTOF otoferlin
OTOG otogelin
OTOGL otogelin-like
P2RX2 purinergic receptor P2X, ligand gated ion channel, 2
PCDH15 protocadherin-related 15
PCNA proliferating cell nuclear antigen
PMP22 peripheral myelin protein 22
PNPT1 polyribonucleotide nucleotidyltransferase 1
POLG polymerase (DNA directed), gamma
PON2 paraoxonase 2
POU3F4 POU class 3 homeobox 4
POU4F3 POU class 4 homeobox 3
PRPH2 peripherin 2 (retinal degeneration, slow)
PRPS1 phosphoribosyl pyrophosphate synthetase 1
PTPRQ protein tyrosine phosphatase, receptor type, Q
RDX radixin
RNR1 RNA, ribosomal cluster 1
RNR2 RNA, ribosomal cluster 2
RSPO1 R-spondin 1
SERPINB6 serpin peptidase inhibitor, clade B (ovalbumin), member 6
SHOX short stature homeobox
SIX1 SIX homeobox 1
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC19A2 solute carrier family 19 (thiamine transporter), member 2
SLC26A1 solute carrier family 26 (anion exchanger), member 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC26A5 solute carrier family 26 (anion exchanger), member 5
SLC29A3 solute carrier family 29 (equilibrative nucleoside transporter), member 3
SLITRK6 SLIT and NTRK-like family, member 6
SMPX small muscle protein, X-linked
SOD1 superoxide dismutase 1, soluble
SOD2 superoxide dismutase 2, mitochondrial
STRC stereocilin
SYNE4 spectrin repeat containing, nuclear envelope family member 4
TBC1D24 TBC1 domain family, member 24
TBX2 T-box 2
TBX4 T-box 4
TECTA tectorin alpha
TFCP2 transcription factor CP2
THRB thyroid hormone receptor, beta
TJP2 tight junction protein 2
TLR2 toll-like receptor 2
TLR4 toll-like receptor 4
TLR9 toll-like receptor 9
TMC1 transmembrane channel-like 1
TMIE transmembrane inner ear
TMPRSS3 transmembrane protease, serine 3
TNC tenascin C
TNF tumor necrosis factor
TPMT thiopurine S-methyltransferase
TPRN taperin
TRIOBP TRIO and F-actin binding protein
TSPEAR thrombospondin-type laminin G domain and EAR repeats
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)
USH1C Usher syndrome 1C (autosomal recessive, severe)
USH2A Usher syndrome 2A (autosomal recessive, mild)
WFS1 Wolfram syndrome 1 (wolframin)
XIAP X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase