autosomal dominant nonsyndromic deafness Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A nonsyndromic deafness characterized by an autosomal dominant inheritance mode. (Human Disease Ontology, DOID_0050564)
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Genes

49 genes co-occuring with the disease autosomal dominant nonsyndromic deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
MYH14 myosin, heavy chain 14, non-muscle 2.12467
MRPS12 mitochondrial ribosomal protein S12 1.9267
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4 1.81736
TECTA tectorin alpha 1.79345
GRHL2 grainyhead-like 2 (Drosophila) 1.67864
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8 1.67683
CEACAM16 carcinoembryonic antigen-related cell adhesion molecule 16 1.54407
CCDC50 coiled-coil domain containing 50 1.53965
TECTB tectorin beta 1.44869
GJB2 gap junction protein, beta 2, 26kDa 1.37338
EMILIN2 elastin microfibril interfacer 2 1.35943
MYO1A myosin IA 1.32803
MRPL12 mitochondrial ribosomal protein L12 1.3276
UBE3B ubiquitin protein ligase E3B 1.31886
COCH cochlin 1.24645
DFNB59 deafness, autosomal recessive 59 1.22995
DIAPH3 diaphanous-related formin 3 1.21522
CRYM crystallin, mu 1.18798
SLC25A6 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 6 1.17421
DFNA5 deafness, autosomal dominant 5 1.1635
POU4F3 POU class 4 homeobox 3 1.12741
GJB3 gap junction protein, beta 3, 31kDa 1.06438
TMC1 transmembrane channel-like 1 1.05639
ESRRB estrogen-related receptor beta 1.01216
OTOF otoferlin 0.925039
ZNF664 zinc finger protein 664 0.882292
RHOA ras homolog family member A 0.871234
MIR96 microRNA 96 0.836837
MIR183 microRNA 183 0.815924
SARS seryl-tRNA synthetase 0.69751
SIX1 SIX homeobox 1 0.677504
AQP3 aquaporin 3 (Gill blood group) 0.654463
FBXO17 F-box protein 17 0.649323
TRPV4 transient receptor potential cation channel, subfamily V, member 4 0.625711
DNAJB1 DnaJ (Hsp40) homolog, subfamily B, member 1 0.617877
MYO7A myosin VIIA 0.60303
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 0.568775
RDX radixin 0.566443
UCN urocortin 0.54393
FGF1 fibroblast growth factor 1 (acidic) 0.519961
GJB6 gap junction protein, beta 6, 30kDa 0.502675
LIG3 ligase III, DNA, ATP-dependent 0.477909
APPL1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1 0.468441
FZD10 frizzled class receptor 10 0.461261
PDGFRB platelet-derived growth factor receptor, beta polypeptide 0.340906
GRIA3 glutamate receptor, ionotropic, AMPA 3 0.308118
C3 complement component 3 0.274021
PARK2 parkin RBR E3 ubiquitin protein ligase 0.258417
HSP90AA1 heat shock protein 90kDa alpha (cytosolic), class A member 1 0.168854