RAD51:Ensemblv90

RAD51 recombinase
OMIM: 179617, ClinGen, DECIPHER

16 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 16 panels
Red RAD51 in Bone Marrow Failure Level 2: Haematological disorders Version 1.131 Component of the following Super Panels: Immunological disorders_SuperPanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert list Phenotypes Fanconi anemia complementation group R MONDO:0014986
Green RAD51 in Chromosome Breakage Disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 1.24	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group R, MIM# 617244
Green RAD51 in Mendeliome Version 1.3802	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Expert Review Green Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group R, MIM# 617244
Amber RAD51 in Radial Ray Abnormalities Level 2: Dysmorphic and congenital abnormality syndromes Version 1.19 Component of the following Super Panels: Limb and Digital Malformations SuperPanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert Review Phenotypes Fanconi anaemia, complementation group R, MIM# 617244
Green RAD51 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.578	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Red RAD51 in NCGC Version 0.3	0 reviews	Other	Sources NCGC Phenotypes NA
Green RAD51 in Growth failure Version 1.87	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Phenotypes Fanconi anaemia, complementation group R, MIM# 617244
Green RAD51 in Mirror movements Level 2: Neurology and neurodevelopmental disorders Version 1.1	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Mirror movements 2 MIM#614508
Green RAD51 in Fetal anomalies Version 1.482	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Expert Review Phenotypes Fanconi anaemia, complementation group R, MIM# 617244
Red RAD51 in Bone Marrow Failure Level 2: Haematological disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Red Phenotypes Fanconi anemia complementation group R MONDO:0014986
Green RAD51 in Chromosome Breakage Disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Fanconi anaemia, complementation group R, MIM# 617244
Amber RAD51 in Radial Ray Abnormalities Level 2: Dysmorphic and congenital abnormality syndromes Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Expert Review Amber Phenotypes Fanconi anaemia, complementation group R, MIM# 617244
Green RAD51 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 1.0	0 reviews	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services
Green RAD51 in Growth failure Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Expert Review Green Phenotypes Fanconi anaemia, complementation group R, MIM# 617244
Green RAD51 in Mirror movements Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes Mirror movements 2 MIM#614508
Green RAD51 in Fetal anomalies Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Genomics England PanelApp Expert Review Green Phenotypes Fanconi anaemia, complementation group R, MIM# 617244