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COVID-19 research

Gene: RAD51

Green List (high evidence)
RAD51 (RAD51 recombinase)
EnsemblGeneIds (GRCh38): ENSG00000051180
EnsemblGeneIds (GRCh37): ENSG00000051180
OMIM: 179617, Gene2Phenotype
RAD51 is in 11 panels

2 reviews

Sophie Hambleton (Newcastle University)

Green List (high evidence)

IUIS gene
Created: 1 May 2020, 12:18 p.m. | Last Modified: 1 May 2020, 12:18 p.m.
Panel Version: 0.171
Created: 1 May 2020, 12:18 p.m.
Last Modified: 1 May 2020, 12:18 p.m.
Panel version: 0.171

Ivone Leong (Genomics England Curator)

Green List (high evidence)

IUIS: categorised under bone marrow failure with immune deficiency - Fanconi Anemia section. Inheritance AR. T cells: normal to low. B cells: normal to low. Other affected cells: HSC. Associated features: Normal to low NK, CNS, skeletal, skin, cardiac, GI, urogenital anomalies, increased chromosomal breakage.
Created: 15 Apr 2020, 12:09 p.m. | Last Modified: 15 Apr 2020, 12:09 p.m.
Panel Version: 0.103

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
?Fanconi anemia, complementation group R, 617244

Publications

Created: 15 Apr 2020, 12:09 p.m.
Last Modified: 15 Apr 2020, 12:09 p.m.
Panel version: 0.103

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • IUIS Classification December 2019
  • Expert Review Green
Phenotypes
  • ?Fanconi anemia, complementation group R, 617244
OMIM
179617
Clinvar variants
Variants in RAD51
Penetrance
None
Publications
Panels with this gene

History Filter Activity

13 Oct 2021, Gel status: 3

Set mode of inheritance

Arina Puzriakova (Genomics England Curator)

Mode of inheritance for gene: RAD51 was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

15 Apr 2020, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Ivone Leong (Genomics England Curator)

gene: RAD51 was added gene: RAD51 was added to Viral susceptibility. Sources: Expert Review Green,IUIS Classification December 2019 Mode of inheritance for gene: RAD51 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: RAD51 were set to 32086639; 32048120 Phenotypes for gene: RAD51 were set to ?Fanconi anemia, complementation group R, 617244