Gene mutations are genetic. Medical search. Frequent questions

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Anatomy10

Cell Line COS Cells X Chromosome Chromosomes, Human, Pair 17 Cell Line, Tumor Cells, Cultured Fibroblasts Tumor Cells, Cultured Chromosomes, Human, X HEK293 Cells

Organisms10

Escherichia coli Saccharomyces cerevisiae Mice, Mutant Strains Mice, Transgenic Drosophila melanogaster Cricetinae Cercopithecus aethiops Mice, Inbred C57BL Drosophila Mice, Knockout

Diseases43

Adenocarcinoma Genetic Predisposition to Disease Syndrome Genetic Diseases, X-Linked Colorectal Neoplasms, Hereditary Nonpolyposis Abnormalities, Multiple Colorectal Neoplasms Retinitis Pigmentosa Eye Abnormalities Adenomatous Polyposis Coli Lung Neoplasms Chromosome Deletion Mitochondrial Diseases Hemochromatosis Genetic Diseases, Inborn Cardiomyopathy, Hypertrophic Breast Neoplasms Cell Transformation, Neoplastic Cardiomyopathy, Hypertrophic, Familial Leukemia, Myeloid, Acute Ovarian Neoplasms Corneal Dystrophies, Hereditary Neoplastic Syndromes, Hereditary Disease Models, Animal Adenoma Hearing Loss, Sensorineural Microsatellite Instability Deafness Osteochondrodysplasias Familial Mediterranean Fever Ectodermal Dysplasia Neoplasms Noonan Syndrome Paraganglioma Urogenital Abnormalities Marfan Syndrome Intellectual Disability Charcot-Marie-Tooth Disease Muscular Dystrophies Cystic Fibrosis Nystagmus, Congenital Albinism, Oculocutaneous Skin Neoplasms

Chemicals and Drugs64

DNA, Neoplasm Codon, Nonsense Codon DNA Primers Proto-Oncogene Proteins B-raf DNA-Binding Proteins Membrane Proteins Tumor Suppressor Protein p53 DNA, Mitochondrial DNA Transcription Factors Nuclear Proteins Mutant Proteins Carrier Proteins Proto-Oncogene Proteins Mutagens Eye Proteins Bacterial Proteins ras Proteins RNA, Messenger MutS Homolog 2 Protein BRCA2 Protein Ethylnitrosourea RNA Splice Sites Cytoskeletal Proteins Proteins Neoplasm Proteins Genetic Markers Isocitrate Dehydrogenase Cystic Fibrosis Transmembrane Conductance Regulator fms-Like Tyrosine Kinase 3 Tumor Suppressor Proteins Hypoxanthine Phosphoribosyltransferase Recombinant Proteins Adaptor Proteins, Signal Transducing Trans-Activators Repressor Proteins DNA, Complementary Saccharomyces cerevisiae Proteins DNA Transposable Elements Homeodomain Proteins BRCA1 Protein Codon, Terminator Factor V Fungal Proteins Receptor, Epidermal Growth Factor Escherichia coli Proteins DNA, Bacterial Protein-Serine-Threonine Kinases Drosophila Proteins Ethyl Methanesulfonate Adenosine Triphosphatases Recombinant Fusion Proteins beta Catenin Nerve Tissue Proteins Lamin Type A Von Hippel-Lindau Tumor Suppressor Protein Receptor, Fibroblast Growth Factor, Type 3 Membrane Transport Proteins Prothrombin Arginine DNA Repair Enzymes Proto-Oncogene Proteins c-ret Ubiquitin-Protein Ligases

Analytical, Diagnostic and Therapeutic Techniques and Equipment31

DNA Mutational Analysis Pedigree Polymerase Chain Reaction Immunohistochemistry Amino Acid Substitution Genetic Testing Sequence Analysis, DNA Mutagenesis, Site-Directed Chromosome Mapping Models, Molecular Models, Genetic Genetic Complementation Test Heterozygote Detection Sequence Alignment Cloning, Molecular Mutagenesis, Insertional Transfection Crosses, Genetic Genetic Association Studies Reverse Transcriptase Polymerase Chain Reaction Case-Control Studies Prognosis Restriction Mapping Mutagenicity Tests Cohort Studies Disease Models, Animal Blotting, Western Models, Biological Blotting, Southern Electroretinography Heteroduplex Analysis

Psychiatry and Psychology2

Family Intellectual Disability

Phenomena and Processes98

Mutation Point Mutation Mutation, Missense Polymorphism, Single-Stranded Conformational Genes, p53 Exons Heterozygote Base Sequence Frameshift Mutation Germ-Line Mutation Phenotype Alleles Amino Acid Substitution Codon, Nonsense Mutation Rate Genotype Homozygote Amino Acid Sequence Genes, Recessive Codon Mutagenesis Sequence Deletion Genes, Dominant Genetic Predisposition to Disease Gene Deletion Suppression, Genetic Genes, ras Protein Structure, Tertiary Founder Effect Polymorphism, Genetic Consanguinity Gene Frequency Genetic Linkage Genes, BRCA1 Sequence Homology, Amino Acid Penetrance Exome Microsatellite Repeats Introns Binding Sites Genetic Variation Polymorphism, Restriction Fragment Length Genes, Lethal Loss of Heterozygosity Genes, APC Plasmids Genes, BRCA2 Protein Binding Mutagenesis, Insertional Transfection Genes RNA Splice Sites Promoter Regions, Genetic Signal Transduction DNA Mismatch Repair Selection, Genetic Recombination, Genetic Transcription, Genetic Genes, Bacterial Polymorphism, Single Nucleotide RNA Splicing DNA Repair Protein Conformation Genes, Fungal Genetic Markers Temperature Evolution, Molecular Gene Expression INDEL Mutation Structure-Activity Relationship Base Pair Mismatch Chromosome Deletion Genetic Heterogeneity X Chromosome Conserved Sequence Gene Expression Regulation, Neoplastic Mosaicism DNA Transposable Elements Drug Resistance, Viral Kinetics Genes, Suppressor Protein Structure, Secondary Chromosomes, Human, Pair 17 Codon, Terminator Genes, Tumor Suppressor Drug Resistance, Microbial Drug Resistance Gene Expression Regulation Gene Dosage Alternative Splicing Gene Amplification Microsatellite Instability Genes, erbB-1 Time Factors Ultraviolet Rays Chromosomes, Human, X Genes, Regulator Phosphorylation

Disciplines and Occupations2

Immunohistochemistry Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups3

Asian Continental Ancestry Group Jews Infant, Newborn

Health Care8

Genetic Testing Family Health Age of Onset Temperature Case-Control Studies Cohort Studies Ultraviolet Rays Genetic Counseling

Geographicals3

China Italy Japan

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 Geographicals

Mutation Point Mutation Mutation, Missense DNA Mutational Analysis Polymorphism, Single-Stranded Conformational Genes, p53 Pedigree Exons Polymerase Chain Reaction Heterozygote Base Sequence Molecular Sequence Data Frameshift Mutation DNA, Neoplasm Germ-Line Mutation Adenocarcinoma Immunohistochemistry Phenotype Alleles Amino Acid Substitution Genetic Testing Codon, Nonsense Mutation Rate Genotype Homozygote Amino Acid Sequence Sequence Analysis, DNA Genes, Recessive Codon Mutagenesis Sequence Deletion Genes, Dominant Mutagenesis, Site-Directed Genetic Predisposition to Disease DNA Primers Gene Deletion Syndrome Chromosome Mapping Proto-Oncogene Proteins B-raf Suppression, Genetic Genes, ras DNA-Binding Proteins Protein Structure, Tertiary Family Health Founder Effect Polymorphism, Genetic Models, Molecular Escherichia coli Membrane Proteins Consanguinity Gene Frequency Genetic Linkage Tumor Suppressor Protein p53 DNA, Mitochondrial Genes, BRCA1 DNA Models, Genetic Transcription Factors Genetic Complementation Test Nuclear Proteins Heterozygote Detection Cell Line Age of Onset Mutant Proteins Sequence Homology, Amino Acid Genetic Diseases, X-Linked Penetrance Exome Microsatellite Repeats Sequence Alignment Carrier Proteins Proto-Oncogene Proteins Introns Saccharomyces cerevisiae Binding Sites Cloning, Molecular Genetic Variation Polymorphism, Restriction Fragment Length Genes, Lethal Loss of Heterozygosity Genes, APC Mutagens Asian Continental Ancestry Group Eye Proteins Plasmids Genes, BRCA2 Protein Binding Mutagenesis, Insertional Bacterial Proteins ras Proteins Transfection RNA, Messenger Genes Jews Colorectal Neoplasms, Hereditary Nonpolyposis MutS Homolog 2 Protein BRCA2 Protein Crosses, Genetic Ethylnitrosourea Abnormalities, Multiple

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