Gene: GRXCR1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1 		0.330 Biomarker disease 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 		0.330 Biomarker disease CLINGEN Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss. 26969326 2016
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1 		0.330 Biomarker disease CLINGEN Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness. 25802247 2015
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1 		0.330 Biomarker disease CLINGEN Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. 26445815 2015
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1 		0.330 Biomarker disease BEFREE 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
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1 		0.330 Biomarker disease 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 		0.330 Biomarker disease 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
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1 		0.330 GeneticVariation disease BEFREE Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment. 20137778 2010
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1 		0.330 GeneticVariation disease BEFREE This region exhibits conserved synteny with human chromosome 4 and suggests that pirouette may be a genetic model of the human nonsyndromic deafness disorder DFNB25, which has been localized to 4p15.3-q12. 15347914 2004