MSRB3:Ensemblv90

methionine sulfoxide reductase B3
OMIM: 613719, ClinGen, DECIPHER

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green MSRB3 in Mendeliome Version 1.3802	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Deafness, autosomal recessive 74, MIM# 613718
Green MSRB3 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.304	1 review	Unknown	Sources Expert Review Green Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Deafness, autosomal recessive 74, MIM# 613718
Green MSRB3 in Deafness_Isolated Level 2: Hearing and ear disorders Version 1.84	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Melbourne Genomics Health Alliance Deafness Flagship Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Deafness, autosomal recessive 74, MIM# 613718
Red MSRB3 in Additional findings_Paediatric Level 2: Screening Version 0.278	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category C gene Phenotypes Deafness, autosomal recessive
Red MSRB3 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.141	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category C gene Expert Review Red Phenotypes Deafness, autosomal recessive
Green MSRB3 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 2.0	1 review	Unknown	Sources Victorian Clinical Genetics Services Melbourne Genomics Health Alliance Deafness Flagship Expert Review Green Phenotypes Deafness, autosomal recessive 74, MIM# 613718
Green MSRB3 in Deafness_Isolated Level 2: Hearing and ear disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Melbourne Genomics Health Alliance Deafness Flagship Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Expert Review Green Phenotypes Deafness, autosomal recessive 74, MIM# 613718