ClinGen Gene Validity Curations

Gene: RAD51D

Red List (low evidence)

RAD51D (RAD51 paralog D)
EnsemblGeneIds (GRCh38): ENSG00000185379
EnsemblGeneIds (GRCh37): ENSG00000185379
OMIM: 602954, Gene2Phenotype
RAD51D is in 6 panels

1 review

Ellen McDonagh (Genomics England Curator)

This gene and information sourced from the ClinGen Gene Validity Curations. For the full report and publications, see the ClinGen Gene Validity Curation for each gene here: https://search.clinicalgenome.org/kb/gene-validity.
Created: 23 Jun 2017, 11:51 a.m.

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • ClinGen
Phenotypes
  • Hereditary breast cancer
  • OrphaNet ORPHA227535
  • OMIM 614291
OMIM
602954
Clinvar variants
Variants in RAD51D
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

22 Jun 2017, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

RAD51D was added to ClinGen Gene Validity Curationspanel. Source: Expert Review Red

20 Jun 2017, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

RAD51D was added to ClinGen Gene Validity Curationspanel. Sources: ClinGen

20 Jun 2017, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

RAD51D was created by ellenmcdonagh