Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.330 Biomarker CLINGEN Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. 26226137

2016
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.330 Biomarker CLINGEN Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss. 26969326

2016
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.330 Biomarker CLINGEN Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness. 25802247

2015
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.330 Biomarker CLINGEN Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. 26445815

2015
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.330 Biomarker CLINGEN Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment. 20137778

2010
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.330 Biomarker CLINGEN We also provide sequence data of GRXCR1 from humans with profound hearing loss suggesting that pirouette is a model for studying the mechanism of nonsyndromic deafness DFNB25. 20137774

2010