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
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
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
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
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
Search interest in RAD51
Potential gene panels for RAD51 gene
Hereditary Myeloid Malignancy and Inherited Bone Marrow Failure Panel Panel
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 panelBreast cancer (sequence analysis of RAD51 gene) Panel
By CGC Genetics
This panel specifically test the RAD51 gene.
More info about this panelHereditary Ovarian Cancer Panel
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 panelFanconi Anemia Sequencing Panel with CNV Detection Panel
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 panelFanconi Anemia via RAD51/FANCR Gene Sequencing with CNV Detection Panel
By PreventionGenetics PreventionGenetics
This panel specifically test the RAD51 gene.
More info about this panelMirror movements, familial congenital Panel
By Centogene AG - the Rare Disease Company
This panel specifically test the RAD51 gene.
More info about this panelBreast ovarian cancer panel Panel
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 panelSingle gene testing RAD51 Panel
By CeGaT GmbH
This panel specifically test the RAD51 gene.
More info about this panelNGS Panel for Fanconi anemia Panel
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 panelHereditary Cancer NGS Panel Panel
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 panelRAD51 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the RAD51 gene.
More info about this panelFocus Cancer Panel - 40 Genes Panel
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 panelComprehensive Cancer Panel Panel
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 panelBREASTON-EXTENDED Panel
By PentaCoreLab BREASTON-EXTENDED that also includes the following genes: BRCA1 BRCA2 STK11 TP53 CDH1 BRIP1 PALB2 ERBB2 KRAS DIRAS3
More info about this panelFoundationOne® Heme Panel
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 panelHereditary Cancer Comprehensive Panel Panel
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 panelNeoTYPE® Discovery Profile for Solid Tumors Panel
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 panelCaris MI TumorSeek 592-Gene NGS Panel Panel
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 panelOtogenetics Hereditary Cancers Panel
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 panelBREAST AND OVARIAN CANCER NGS PANEL Panel
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 panelFamilial Congenital Mirror Movements, Massive Sequencing (NGS) DCC, RAD51 Genes Panel
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 panel152 Integrated Advantage NGS Solid Tumor Panel Panel
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 panelTempus xT assay Panel
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 panelTempus xO assay Panel
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 panelFanconi Anemia: gene sequencing panel Panel
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 panelEsophageal Atresia/Tracheoesophageal Fistula: gene sequencing panel Panel
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
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