Apc germline mutations are frameshift. Medical search. Frequent questions

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Anatomy2

Germ Cells Cell Line

Organisms3

Escherichia coli Caenorhabditis elegans Saccharomyces cerevisiae

Diseases27

Adenomatous Polyposis Coli Neoplastic Syndromes, Hereditary Colorectal Neoplasms, Hereditary Nonpolyposis Paraganglioma Genetic Predisposition to Disease Hamartoma Syndrome, Multiple Li-Fraumeni Syndrome Peutz-Jeghers Syndrome Syndrome Microsatellite Instability Multiple Endocrine Neoplasia Type 2a Intestinal Polyposis Pheochromocytoma Colorectal Neoplasms von Hippel-Lindau Disease Noonan Syndrome Paraganglioma, Extra-Adrenal Breast Neoplasms Ovarian Neoplasms Costello Syndrome Carcinoma, Medullary Leiomyomatosis Adrenal Gland Neoplasms Multiple Endocrine Neoplasia Type 1 Abnormalities, Multiple Adenoma Neoplasms, Multiple Primary

Chemicals and Drugs33

MutS Homolog 2 Protein BRCA2 Protein Codon, Nonsense Codon Adenomatous Polyposis Coli Protein DNA, Neoplasm DNA-Binding Proteins Nuclear Proteins BRCA1 Protein Proto-Oncogene Proteins c-ret Adaptor Proteins, Signal Transducing Succinate Dehydrogenase Proto-Oncogene Proteins Neoplasm Proteins DNA Primers Fumarate Hydratase Tumor Suppressor Proteins Transcription Factors Carrier Proteins DNA Drosophila Proteins PTEN Phosphohydrolase RNA, Messenger Proto-Oncogene Proteins B-raf RNA Splice Sites Codon, Terminator Tumor Suppressor Protein p53 Membrane Proteins Von Hippel-Lindau Tumor Suppressor Protein Protein-Serine-Threonine Kinases DNA Repair Enzymes Mutant Proteins Genetic Markers

Analytical, Diagnostic and Therapeutic Techniques and Equipment16

DNA Mutational Analysis Pedigree Genetic Testing Polymerase Chain Reaction Sequence Analysis, DNA Amino Acid Substitution Heterozygote Detection Models, Genetic Mutagenesis, Site-Directed Chromosome Mapping Cloning, Molecular Models, Molecular Mutagenesis, Insertional Genetic Complementation Test Sequence Alignment Immunohistochemistry

Psychiatry and Psychology1

Phenomena and Processes60

Germ-Line Mutation Genes, APC Frameshift Mutation Mutation Mutation, Missense Point Mutation Base Sequence Exons Genes, BRCA1 Heterozygote Frameshifting, Ribosomal Polymorphism, Single-Stranded Conformational Phenotype Alleles Genetic Predisposition to Disease Codon, Nonsense Amino Acid Sequence Genes, BRCA2 Mutation Rate Sequence Deletion DNA Mismatch Repair Loss of Heterozygosity Microsatellite Repeats Codon Genotype Homozygote Amino Acid Substitution Penetrance Mutagenesis Base Pair Mismatch Founder Effect Genes, p53 Microsatellite Instability Gene Deletion Genes, Recessive Genes, Dominant Suppression, Genetic Polymorphism, Genetic Exome DNA Repair Gene Frequency Mosaicism Genetic Linkage Protein Structure, Tertiary Sequence Homology, Amino Acid Consanguinity Introns RNA Splice Sites Genetic Variation Mutagenesis, Insertional Genes, Tumor Suppressor Codon, Terminator Genes, p16 Signal Transduction Promoter Regions, Genetic Polymorphism, Single Nucleotide Transcription, Genetic Recombination, Genetic Plasmids Genetic Markers

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

Named Groups1

Health Care3

Genetic Testing Family Health Age of Onset

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

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

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