Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5962
Gene Symbol: RDX
RDX
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.310 Biomarker CLINGEN Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. 26226137

2016

Entrez Id: 5962
Gene Symbol: RDX
RDX
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.310 Biomarker CLINGEN CLIC5 stabilizes membrane-actin filament linkages at the base of hair cell stereocilia in a molecular complex with radixin, taperin, and myosin VI. 24285636

2014

Entrez Id: 5962
Gene Symbol: RDX
RDX
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.310 Biomarker CLINGEN Molecular architecture of the chick vestibular hair bundle. 23334578

2013

Entrez Id: 5962
Gene Symbol: RDX
RDX
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.310 Biomarker CLINGEN Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX Gene. 22567349

2011

Entrez Id: 5962
Gene Symbol: RDX
RDX
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.310 Biomarker CLINGEN A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family. 19215054

2009

Entrez Id: 5962
Gene Symbol: RDX
RDX
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.310 Biomarker CLINGEN Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus. 17226784

2007

Entrez Id: 5962
Gene Symbol: RDX
RDX
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.310 Biomarker CLINGEN Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia. 15314067

2004

Entrez Id: 5962
Gene Symbol: RDX
RDX
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
0.310 Biomarker CLINGEN Radixin is a constituent of stereocilia in hair cells. 14983055

2004