Germline mutations in brca1 or brca2 genes. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy11

Germ Cells Cell Line Cell Line, Tumor Chromosomes, Human, Pair 17 Tumor Cells, Cultured Micronucleus, Germline Cell Nucleus Ovary Cells, Cultured Stem Cells HeLa Cells

Organisms10

Caenorhabditis elegans Drosophila melanogaster Drosophila Animals, Genetically Modified Mice, Mutant Strains Escherichia coli Mice, Transgenic Mice, Knockout Saccharomyces cerevisiae Mice, Inbred C57BL

Diseases61

Neoplastic Syndromes, Hereditary Genetic Predisposition to Disease Colorectal Neoplasms, Hereditary Nonpolyposis Breast Neoplasms Ovarian Neoplasms Paraganglioma Hamartoma Syndrome, Multiple Adenomatous Polyposis Coli Li-Fraumeni Syndrome Peutz-Jeghers Syndrome Multiple Endocrine Neoplasia Type 2a Intestinal Polyposis von Hippel-Lindau Disease Breast Neoplasms, Male Pheochromocytoma Paraganglioma, Extra-Adrenal Syndrome Noonan Syndrome Costello Syndrome Microsatellite Instability Carcinoma, Medullary Leiomyomatosis Adrenal Gland Neoplasms Multiple Endocrine Neoplasia Type 1 Colorectal Neoplasms Neoplasms, Multiple Primary Genomic Instability Adenoma Abnormalities, Multiple Melanoma Retinoblastoma Birt-Hogg-Dube Syndrome Neoplasms Hemangioblastoma Thyroid Neoplasms Retinal Neoplasms Facies Carcinoma Skin Neoplasms Endometrial Neoplasms LEOPARD Syndrome Cell Transformation, Neoplastic Sebaceous Gland Neoplasms Pancreatic Neoplasms Hirschsprung Disease Craniofacial Abnormalities Adenocarcinoma Ectodermal Dysplasia Growth Hormone-Secreting Pituitary Adenoma Intestinal Polyps Multiple Endocrine Neoplasia Type 2b Neurofibromatosis 1 Skin Abnormalities Hereditary Breast and Ovarian Cancer Syndrome Kidney Neoplasms Abdominal Neoplasms Fallopian Tube Neoplasms Neurofibromatoses Dysplastic Nevus Syndrome Stomach Neoplasms Carotid Body Tumor

Chemicals and Drugs53

BRCA1 Protein BRCA2 Protein MutS Homolog 2 Protein Neoplasm Proteins DNA, Neoplasm Nuclear Proteins DNA-Binding Proteins Tumor Suppressor Proteins Proto-Oncogene Proteins c-ret Transcription Factors Succinate Dehydrogenase Codon, Nonsense Adaptor Proteins, Signal Transducing Fumarate Hydratase Proto-Oncogene Proteins Codon Carrier Proteins DNA Primers Rad51 Recombinase Tumor Suppressor Protein p53 Drosophila Proteins PTEN Phosphohydrolase DNA Protein-Serine-Threonine Kinases Genetic Markers Ubiquitin-Protein Ligases Von Hippel-Lindau Tumor Suppressor Protein DNA Repair Enzymes RNA, Messenger Proto-Oncogene Proteins B-raf RNA Splice Sites Caenorhabditis elegans Proteins Mutant Proteins Membrane Proteins Cyclin-Dependent Kinase Inhibitor p16 Adenomatous Polyposis Coli Protein Cell Cycle Proteins Checkpoint Kinase 2 Phosphoric Monoester Hydrolases Proteins DNA Glycosylases Receptor Protein-Tyrosine Kinases Electron Transport Complex II Intracellular Signaling Peptides and Proteins Immunoglobulin Variable Region ras Proteins Adenosine Triphosphatases Cadherins Tumor Markers, Biological Californium Apoptosis Regulatory Proteins Repressor Proteins DNA Transposable Elements

Analytical, Diagnostic and Therapeutic Techniques and Equipment35

Pedigree DNA Mutational Analysis Genetic Testing Polymerase Chain Reaction Sequence Analysis, DNA Heterozygote Detection Amino Acid Substitution Case-Control Studies Models, Genetic Immunohistochemistry Mutagenesis, Site-Directed Chromosome Mapping Models, Molecular Mutagenesis, Insertional Transfection Cohort Studies Risk Factors Facies Reverse Transcriptase Polymerase Chain Reaction Genetic Association Studies Sequence Alignment Cloning, Molecular Genetic Complementation Test Salpingectomy Prognosis Risk Heteroduplex Analysis Comparative Genomic Hybridization Gene Targeting Gene Expression Profiling Models, Biological Blotting, Western Crosses, Genetic Blotting, Southern Risk Assessment

Psychiatry and Psychology1

Phenomena and Processes87

Genes, BRCA1 Genes, BRCA2 Germ-Line Mutation Mutation Mutation, Missense Point Mutation Frameshift Mutation Heterozygote Genetic Predisposition to Disease Exons Polymorphism, Single-Stranded Conformational Founder Effect Base Sequence Alleles Mutation Rate Loss of Heterozygosity Phenotype DNA Mismatch Repair Penetrance Genotype Microsatellite Repeats Genes, APC Sequence Deletion DNA Repair Codon, Nonsense Genes, p53 Amino Acid Sequence Amino Acid Substitution Microsatellite Instability Base Pair Mismatch Gene Deletion Homozygote Codon Gene Frequency Polymorphism, Genetic Genes, Tumor Suppressor Mutagenesis Protein Structure, Tertiary Promoter Regions, Genetic Mosaicism Genes, p16 Gene Expression Regulation, Neoplastic DNA Damage Genetic Markers Polymorphism, Single Nucleotide Genes, Recessive Genes, Dominant Exome Genomic Instability Genetic Variation Recombination, Genetic Genetic Linkage DNA Methylation Signal Transduction Introns Sequence Homology, Amino Acid Oogenesis Transcription, Genetic Protein Binding RNA Splice Sites Mutagenesis, Insertional Transfection Binding Sites Genetic Heterogeneity Gene Silencing Genes, Neurofibromatosis 1 Consanguinity Haplotypes Chromosomes, Human, Pair 17 Gene Rearrangement Suppression, Genetic Haploinsufficiency Genes, Lethal Heredity Homologous Recombination Gene Expression Regulation Risk Immunoglobulin Variable Region Plasmids Gene Expression Regulation, Developmental Alternative Splicing Genes, X-Linked Phosphorylation Genes, Immunoglobulin Cell Division Genome, Human DNA Transposable Elements

Disciplines and Occupations2

Genetic Counseling Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups2

Jews Asian Continental Ancestry Group

Health Care9

Genetic Testing Family Health Age of Onset Genetic Counseling Case-Control Studies Cohort Studies Risk Factors Risk Risk Assessment

Geographicals2

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care

BRCA1 Protein Genes, BRCA1 BRCA2 Protein Genes, BRCA2 Germ-Line Mutation Mutation Mutation, Missense Point Mutation Pedigree DNA Mutational Analysis Neoplastic Syndromes, Hereditary Genetic Testing Frameshift Mutation Heterozygote Genetic Predisposition to Disease Colorectal Neoplasms, Hereditary Nonpolyposis Breast Neoplasms Ovarian Neoplasms Exons MutS Homolog 2 Protein Paraganglioma Jews Polymorphism, Single-Stranded Conformational Hamartoma Syndrome, Multiple Founder Effect Base Sequence Adenomatous Polyposis Coli Germ Cells Alleles Mutation Rate Li-Fraumeni Syndrome Polymerase Chain Reaction Loss of Heterozygosity Molecular Sequence Data Phenotype Family Health Neoplasm Proteins DNA Mismatch Repair DNA, Neoplasm Nuclear Proteins Penetrance DNA-Binding Proteins Genotype Peutz-Jeghers Syndrome Tumor Suppressor Proteins Sequence Analysis, DNA Microsatellite Repeats Genes, APC Sequence Deletion Age of Onset DNA Repair Proto-Oncogene Proteins c-ret Transcription Factors Succinate Dehydrogenase Heterozygote Detection Codon, Nonsense Multiple Endocrine Neoplasia Type 2a Adaptor Proteins, Signal Transducing Genetic Counseling Genes, p53 Amino Acid Sequence Intestinal Polyposis von Hippel-Lindau Disease Amino Acid Substitution Breast Neoplasms, Male Pheochromocytoma Fumarate Hydratase Paraganglioma, Extra-Adrenal Syndrome Noonan Syndrome Costello Syndrome Proto-Oncogene Proteins Microsatellite Instability Carcinoma, Medullary Leiomyomatosis Base Pair Mismatch Gene Deletion Homozygote Codon Carrier Proteins Adrenal Gland Neoplasms Gene Frequency DNA Primers Polymorphism, Genetic Rad51 Recombinase Tumor Suppressor Protein p53 Multiple Endocrine Neoplasia Type 1 Colorectal Neoplasms Genes, Tumor Suppressor Neoplasms, Multiple Primary Mutagenesis Family Drosophila Proteins Protein Structure, Tertiary PTEN Phosphohydrolase Promoter Regions, Genetic Case-Control Studies Mosaicism Genes, p16 DNA

No FAQ available that match "germline mutations in brca1 or brca2 genes"