RAD51 gene related symptoms and diseases

All the information presented here about the RAD51 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,ORPHANET,NCBIGENE, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to RAD51 gene

Symptoms // Phenotype % Cases
Carcinoma Uncommon - Between 30% and 50% cases
Neoplasm Uncommon - Between 30% and 50% cases
Pain Uncommon - Between 30% and 50% cases
Intellectual disability Uncommon - Between 30% and 50% cases
Prostate cancer Uncommon - Between 30% and 50% cases

Other less frequent symptoms and clinical features

Patients with RAD51 gene alterations may also develop some of the following symptoms and phenotypes:
  • Not very common - Between 30% and 50% cases

  • Breast carcinoma
  • Microcephaly
  • Ovarian neoplasm
  • Bimanual synkinesia
  • Chromosome breakage
  • Bone marrow hypocellularity
  • Anal atresia
  • Hydrocephalus

And 188 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to RAD51 gene

Here you will find a list of rare diseases related to the RAD51. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


FANCONI ANEMIA, COMPLEMENTATION GROUP R; FANCR

Most common symptoms of FANCONI ANEMIA, COMPLEMENTATION GROUP R; FANCR

  • Intellectual disability
  • Microcephaly
  • Growth delay
  • Anemia
  • Hydrocephalus


More info about FANCONI ANEMIA, COMPLEMENTATION GROUP R; FANCR

SOURCES: OMIM

FANCONI ANEMIA

Alternate names

FANCONI ANEMIA Is also known as fanconi pancytopenia, fanconi anemia, fa

Description

Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors.

Most common symptoms of FANCONI ANEMIA

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Hearing impairment
  • Microcephaly


More info about FANCONI ANEMIA

SOURCES: OMIM ORPHANET

HEREDITARY BREAST AND OVARIAN CANCER SYNDROME

Description

Breast cancer (BC) is the most common cancer in women, accounting for 25% of all new cases of cancer. Most BC cases are sporadic, while 5-10% are estimated to be due to an inherited predisposition.

Most common symptoms of HEREDITARY BREAST AND OVARIAN CANCER SYNDROME

  • Neoplasm
  • Carcinoma
  • Melanoma
  • Breast carcinoma
  • Ovarian neoplasm


More info about HEREDITARY BREAST AND OVARIAN CANCER SYNDROME

SOURCES: OMIM ORPHANET

BREAST CANCER

Alternate names

BREAST CANCER Is also known as breast cancer, familial

Description

Breast cancer (referring to mammary carcinoma, not mammary sarcoma) is histopathologically and almost certainly etiologically and genetically heterogeneous. Important genetic factors have been indicated by familial occurrence and bilateral involvement.

Most common symptoms of BREAST CANCER

  • Neoplasm
  • Pain
  • Carcinoma
  • Gynecomastia
  • Breast carcinoma


More info about BREAST CANCER

SOURCES: ORPHANET OMIM

FAMILIAL CONGENITAL MIRROR MOVEMENTS

Alternate names

FAMILIAL CONGENITAL MIRROR MOVEMENTS Is also known as hereditary congenital controlateral synkinesia, isolated congenital controlateral synkinesia, hereditary congenital mirror movements, isolated congenital mirror movements, familial congenital controlateral synkinesia

Most common symptoms of FAMILIAL CONGENITAL MIRROR MOVEMENTS

  • Pain
  • Intellectual disability, mild
  • Agenesis of corpus callosum
  • Myalgia
  • Abnormality of movement


More info about FAMILIAL CONGENITAL MIRROR MOVEMENTS

SOURCES: ORPHANET OMIM

MIRROR MOVEMENTS 2; MRMV2

Description

Mirror movements are involuntary movements of a side of the body that mirror intentional movements on the opposite side. Mild mirror movements are physiologic in young children and gradually disappear within the first decade of life, likely due to maturation of the motor network. Mirror movements that persist beyond age 10 years represent a rare disorder usually showing autosomal dominant inheritance with incomplete penetrance (summary by Depienne et al., 2012).For a discussion of genetic heterogeneity of mirror movements, see MRMV1 (OMIM ).

Most common symptoms of MIRROR MOVEMENTS 2; MRMV2

  • Pain
  • Involuntary movements
  • Bimanual synkinesia


More info about MIRROR MOVEMENTS 2; MRMV2

SOURCES: OMIM


Potential gene panels for RAD51 gene

Hereditary Myeloid Malignancy and Inherited Bone Marrow Failure Panel Panel

United States.

By Genetic Services Laboratory University of Chicago Hereditary Myeloid Malignancy and Inherited Bone Marrow Failure Panel that also includes the following genes: RPL11 RPL15 RPL26 RPL35A RPL5 RPS10 RPS19 RPS24 RPS26 RPS7

More info about this panel
United States.

Breast cancer (sequence analysis of RAD51 gene) Panel

Portugal.

By CGC Genetics

This panel specifically test the RAD51 gene.

More info about this panel
Portugal.

Hereditary Ovarian Cancer Panel

Poland.

By Laboratory of Genetics BioTe21 Adam Master Hereditary Ovarian Cancer that also includes the following genes: BRCA1 BRCA2 TP53 BRIP1 MRE11 NBN BARD1 RAD50 RAD51 RAD51C

More info about this panel
Poland.

Fanconi Anemia Sequencing Panel with CNV Detection Panel

United States.

By PreventionGenetics PreventionGenetics Fanconi Anemia Sequencing Panel with CNV Detection that also includes the following genes: BRCA1 BRCA2 XRCC2 BRIP1 FANCL FANCM SLX4 UBE2T FANCI PALB2

More info about this panel
United States.

Fanconi Anemia via RAD51/FANCR Gene Sequencing with CNV Detection Panel

United States.

By PreventionGenetics PreventionGenetics

This panel specifically test the RAD51 gene.

More info about this panel
United States.

Mirror movements, familial congenital Panel

Germany.

By Centogene AG - the Rare Disease Company

This panel specifically test the RAD51 gene.

More info about this panel
Germany.

Breast ovarian cancer panel Panel

Germany.

By Centogene AG - the Rare Disease Company Breast ovarian cancer panel that also includes the following genes: STK11 TP53 CDH1 BRIP1 PALB2 MRE11 MSH6 NBN ATM BARD1

More info about this panel
Germany.

Single gene testing RAD51 Panel

Germany.

By CeGaT GmbH

This panel specifically test the RAD51 gene.

More info about this panel
Germany.

NGS Panel for Fanconi anemia Panel

Spain.

By BLOODGENETICS BLOODGENETICS NGS Panel for Fanconi anemia that also includes the following genes: BRCA1 BRCA2 XRCC2 BRIP1 FANCL FANCM SLX4 UBE2T RFWD3 FANCI

More info about this panel
Spain.

Hereditary Cancer NGS Panel Panel

United States.

By Fulgent Genetics Fulgent Genetics Hereditary Cancer NGS Panel that also includes the following genes: ROBO2 BLM SDHA SDHB SDHC SDHD BMPR1A BRCA1 BRCA2 SMARCB1

More info about this panel
United States.

RAD51 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the RAD51 gene.

More info about this panel
United States.

Focus Cancer Panel - 40 Genes Panel

United States.

By Fulgent Genetics Fulgent Genetics Focus Cancer Panel - 40 Genes that also includes the following genes: BMPR1A BRCA1 BRCA2 STK11 EPCAM TP53 VHL CDH1 CDK4 CDKN2A

More info about this panel
United States.

Comprehensive Cancer Panel Panel

United States.

By Fulgent Genetics Fulgent Genetics Comprehensive Cancer Panel that also includes the following genes: ROBO2 RUNX1 BLM SDHA SDHB SDHC SDHD BMPR1A BRCA1 BRCA2

More info about this panel
United States.

BREASTON-EXTENDED Panel

Hungary.

By PentaCoreLab BREASTON-EXTENDED that also includes the following genes: BRCA1 BRCA2 STK11 TP53 CDH1 BRIP1 PALB2 ERBB2 KRAS DIRAS3

More info about this panel
Hungary.

FoundationOne® Heme Panel

United States.

By Foundation Medicine, Inc. FoundationOne® Heme that also includes the following genes: BCL6 BCL7A ROS1 RUNX1 BLM SDHA SDHB SDHC SDHD SF3B1

More info about this panel
United States.

Hereditary Cancer Comprehensive Panel Panel

United States.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. Hereditary Cancer Comprehensive Panel that also includes the following genes: RUNX1 SDHB SDHC SDHD BMPR1A BRCA1 BRCA2 STK11 EPCAM TERC

More info about this panel
United States.

NeoTYPE® Discovery Profile for Solid Tumors Panel

United States.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. NeoTYPE® Discovery Profile for Solid Tumors that also includes the following genes: BCL6 ROS1 RUNX1 BLM SDHA SDHB SDHC SDHD SF3B1 FOXL2

More info about this panel
United States.

Caris MI TumorSeek 592-Gene NGS Panel Panel

United States.

By Caris Life Sciences Caris MI TumorSeek 592-Gene NGS Panel that also includes the following genes: BCL6 BCL7A BCL9 BCR ROS1 RPL10 RPL22 RPL5 RPN1 RUNX1

More info about this panel
United States.

Otogenetics Hereditary Cancers Panel

United States.

By Otogenetics Otogenetics Hereditary Cancers that also includes the following genes: BMPR1A BRCA1 BRCA2 STK11 EPCAM TP53 VHL ELAC2 PALLD CDH1

More info about this panel
United States.

BREAST AND OVARIAN CANCER NGS PANEL Panel

Spain.

By Laboratorio de Genetica Clinica SL BREAST AND OVARIAN CANCER NGS PANEL that also includes the following genes: BLM BRCA1 BRCA2 STK11 EPCAM TP53 WRN CDH1 PSMC3IP TNFRSF13B

More info about this panel
Spain.

Familial Congenital Mirror Movements, Massive Sequencing (NGS) DCC, RAD51 Genes Panel

Spain.

By Reference Laboratory Genetics Familial Congenital Mirror Movements, Massive Sequencing (NGS) DCC, RAD51 Genes that also includes the following genes: DCC RAD51

More info about this panel
Spain.

152 Integrated Advantage NGS Solid Tumor Panel Panel

United States.

By Integrated Molecular Diagnostics Pathology, Inc. 152 Integrated Advantage NGS Solid Tumor Panel that also includes the following genes: ROS1 RRM1 SLCO1B1 BRAF BRCA1 SLC29A1 BRCA2 SMO SPARC SRC

More info about this panel
United States.

Tempus xT assay Panel

United States.

By Tempus Labs, Inc. Tempus xT assay that also includes the following genes: BCL6 RIT1 BCL7A BCR ROS1 RPL5 RPS15 RPS6KB1 RUNX1 RXRA

More info about this panel
United States.

Tempus xO assay Panel

United States.

By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2

More info about this panel
United States.

Fanconi Anemia: gene sequencing panel Panel

Canada.

By CEN4GEN Institute for Genomics and Molecular Diagnostics Fanconi Anemia: gene sequencing panel that also includes the following genes: BRCA2 XRCC2 BRIP1 FANCL FANCM SLX4 UBE2T RFWD3 FANCI PALB2

More info about this panel
Canada.

Esophageal Atresia/Tracheoesophageal Fistula: gene sequencing panel Panel

Canada.

By CEN4GEN Institute for Genomics and Molecular Diagnostics Esophageal Atresia/Tracheoesophageal Fistula: gene sequencing panel that also includes the following genes: BRCA2 SOX2 XRCC2 BRIP1 CHD7 FANCL FANCM SLX4 UBE2T RFWD3

More info about this panel
Canada.

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