auditory system disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

76 genes involed in the disease auditory system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ACTG1 actin gamma 1
ADCY1 adenylate cyclase 1 (brain)
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
CABP2 calcium binding protein 2
CCDC50 coiled-coil domain containing 50
CDH23 cadherin-related 23
CEACAM16 carcinoembryonic antigen-related cell adhesion molecule 16
CIB2 calcium and integrin binding family member 2
CLDN14 claudin 14
COCH cochlin
COL11A2 collagen, type XI, alpha 2
COL11A2P1 collagen, type XI, alpha 2 pseudogene 1
COL4A6 collagen, type IV, alpha 6
DFNA5 deafness, autosomal dominant 5
DFNB31 deafness, autosomal recessive 31
DFNB59 deafness, autosomal recessive 59
DIABLO diablo, IAP-binding mitochondrial protein
DIAPH1 diaphanous-related formin 1
DIAPH3 diaphanous-related formin 3
ELMOD3 ELMO/CED-12 domain containing 3
ESPN espin
ESRRB estrogen-related receptor beta
EYA4 EYA transcriptional coactivator and phosphatase 4
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB6 gap junction protein, beta 6, 30kDa
GRHL2 grainyhead-like 2 (Drosophila)
GRXCR1 glutaredoxin, cysteine rich 1
GRXCR2 glutaredoxin, cysteine rich 2
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
ILDR1 immunoglobulin-like domain containing receptor 1
KARS lysyl-tRNA synthetase
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4
LHFPL5 lipoma HMGIC fusion partner-like 5
LOXHD1 lipoxygenase homology domains 1
MARVELD2 MARVEL domain containing 2
MSRB3 methionine sulfoxide reductase B3
MYH14 myosin, heavy chain 14, non-muscle
MYH9 myosin, heavy chain 9, non-muscle
MYO15A myosin XVA
MYO1A myosin IA
MYO3A myosin IIIA
MYO6 myosin VI
MYO7A myosin VIIA
OTOA otoancorin
OTOF otoferlin
OTOG otogelin
OTOGL otogelin-like
P2RX2 purinergic receptor P2X, ligand gated ion channel, 2
PCDH15 protocadherin-related 15
PNPT1 polyribonucleotide nucleotidyltransferase 1
POU3F4 POU class 3 homeobox 4
POU4F3 POU class 4 homeobox 3
PRPS1 phosphoribosyl pyrophosphate synthetase 1
PTPRQ protein tyrosine phosphatase, receptor type, Q
RDX radixin
SERPINB6 serpin peptidase inhibitor, clade B (ovalbumin), member 6
SIX1 SIX homeobox 1
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC26A5 solute carrier family 26 (anion exchanger), member 5
SMPX small muscle protein, X-linked
STRC stereocilin
STRCP1 stereocilin pseudogene 1
SYNE4 spectrin repeat containing, nuclear envelope family member 4
TBC1D24 TBC1 domain family, member 24
TECTA tectorin alpha
TMC1 transmembrane channel-like 1
TMIE transmembrane inner ear
TMPRSS3 transmembrane protease, serine 3
TNC tenascin C
TPRN taperin
TRIOBP TRIO and F-actin binding protein
TSPEAR thrombospondin-type laminin G domain and EAR repeats
USH1C Usher syndrome 1C (autosomal recessive, severe)
WFS1 Wolfram syndrome 1 (wolframin)