x-linked 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 X-linked inheritance mode. (Human Disease Ontology, DOID_0050566)
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20 genes co-occuring with the disease x-linked nonsyndromic deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
POU3F4 POU class 3 homeobox 4 3.00834
PRPS1 phosphoribosyl pyrophosphate synthetase 1 1.66149
TIMM8A translocase of inner mitochondrial membrane 8 homolog A (yeast) 1.63142
DCBLD2 discoidin, CUB and LCCL domain containing 2 1.52908
COBLL1 cordon-bleu WH2 repeat protein-like 1 1.50579
RPS6KA6 ribosomal protein S6 kinase, 90kDa, polypeptide 6 1.39914
RAB40AL RAB40A, member RAS oncogene family-like 1.35071
KALRN kalirin, RhoGEF kinase 1.29746
GJB2 gap junction protein, beta 2, 26kDa 0.817976
CHM choroideremia (Rab escort protein 1) 0.793771
COL4A5 collagen, type IV, alpha 5 0.756156
GK glycerol kinase 0.737054
SULT2B1 sulfotransferase family, cytosolic, 2B, member 1 0.706754
GJB6 gap junction protein, beta 6, 30kDa 0.571495
PGRMC1 progesterone receptor membrane component 1 0.55945
BTK Bruton agammaglobulinemia tyrosine kinase 0.451454
SOX2 SRY (sex determining region Y)-box 2 0.419892
PAX2 paired box 2 0.409414
FMR1 fragile X mental retardation 1 0.321909
NDP Norrie disease (pseudoglioma) 0.166095