Gene: MSRB3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 253827
Gene Symbol: MSRB3
MSRB3 		0.600 Biomarker phenotype GENOMICS_ENGLAND Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells. 24191262 2014
Entrez Id: 253827
Gene Symbol: MSRB3
MSRB3 		0.600 Biomarker phenotype CTD_human Recently, several mutations in apoptosis genes were identified as the cause of monogenic hearing impairment.These genes are TJP2, DFNA5 and MSRB3. 21782914 2011
Entrez Id: 253827
Gene Symbol: MSRB3
MSRB3 		0.600 Biomarker phenotype HPO
Entrez Id: 253827
Gene Symbol: MSRB3
MSRB3 		0.600 CausalMutation phenotype CLINVAR