Gene: GRXCR2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 643226
Gene Symbol: GRXCR2
GRXCR2 		0.300 Biomarker disease CLINGEN Grxcr2 is required for stereocilia morphogenesis in the cochlea. 30157177 2018
Entrez Id: 643226
Gene Symbol: GRXCR2
GRXCR2 		0.300 Biomarker disease CLINGEN GRXCR2 Regulates Taperin Localization Critical for Stereocilia Morphology and Hearing. 30380417 2018
Entrez Id: 643226
Gene Symbol: GRXCR2
GRXCR2 		0.300 Biomarker disease CLINGEN A frameshift mutation in GRXCR2 causes recessively inherited hearing loss. 24619944 2014