Found frameshift mutation. Medical search. Frequent questions

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Anatomy2

Cell Line COS Cells

Organisms3

Escherichia coli Saccharomyces cerevisiae Salmonella typhimurium

Diseases17

Syndrome Abnormalities, Multiple Microsatellite Instability Retinitis Pigmentosa Genetic Diseases, X-Linked Paraparesis, Spastic Chromosome Deletion Tooth Abnormalities Colorectal Neoplasms Genetic Predisposition to Disease Cutis Laxa Intellectual Disability Eye Abnormalities Albinism, Oculocutaneous Keratoderma, Palmoplantar Colorectal Neoplasms, Hereditary Nonpolyposis Ectodermal Dysplasia

Chemicals and Drugs43

Codon, Nonsense Codon Codon, Terminator Aminacrine Proflavine Mutagens DNA Primers DNA-Binding Proteins Bacterial Proteins Acridines DNA RNA, Messenger DEFICIENS Protein RNA Splice Sites Transcription Factors Activin Receptors, Type II Carrier Proteins DNA, Neoplasm Membrane Proteins DNA, Bacterial Nuclear Proteins 2-Acetylaminofluorene DNA-Directed DNA Polymerase Anticodon Aminoacridines Escherichia coli Proteins Fusion Proteins, gag-pol MutS Homolog 2 Protein DNA, Complementary Oligonucleotide Probes DNA Transposable Elements Eye Proteins DNA, Viral Receptors, Transforming Growth Factor beta Proteins Nucleic Acid Heteroduplexes Proto-Oncogene Proteins DNA, Mitochondrial RNA, Viral Nitrogen Mustard Compounds Pregnenes Neoplasm Proteins Saccharomyces cerevisiae Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment19

Pedigree DNA Mutational Analysis Polymerase Chain Reaction Sequence Analysis, DNA Cloning, Molecular Mutagenesis, Site-Directed Amino Acid Substitution Genetic Complementation Test Chromosome Mapping Sequence Alignment Mutagenesis, Insertional Restriction Mapping Genetic Testing Models, Genetic Transfection Models, Molecular Mutagenicity Tests Reverse Transcriptase Polymerase Chain Reaction Genetic Association Studies

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes82

Frameshift Mutation Mutation Point Mutation Mutation, Missense Base Sequence Frameshifting, Ribosomal Codon, Nonsense Exons Amino Acid Sequence Germ-Line Mutation Phenotype Sequence Deletion Alleles Heterozygote Homozygote Polymorphism, Single-Stranded Conformational Microsatellite Repeats Codon Suppression, Genetic Mutagenesis Genes, Recessive Codon, Terminator Gene Deletion Base Pair Mismatch Genotype Consanguinity Plasmids Open Reading Frames Genes, Bacterial Amino Acid Substitution Mutation Rate Genes, Dominant DNA Repair Sequence Homology, Amino Acid Reading Frames Exome Genes Genetic Linkage RNA Splice Sites Mutagenesis, Insertional Protein Structure, Tertiary Microsatellite Instability Founder Effect Recombination, Genetic Protein Biosynthesis Transcription, Genetic Introns Transfection Nucleic Acid Conformation Sequence Homology, Nucleic Acid Chromosome Deletion Genes, p53 DNA Replication Polymorphism, Genetic Pseudogenes Repetitive Sequences, Nucleic Acid Anticodon Operon Genes, Suppressor Genetic Predisposition to Disease DNA Mismatch Repair RNA Splicing Genetic Variation Binding Sites Conserved Sequence Lac Operon Gene Expression Regulation, Bacterial Genes, APC Loss of Heterozygosity Genes, BRCA1 DNA Transposable Elements Haploinsufficiency Promoter Regions, Genetic Genes, Viral Gene Expression Genetic Code Genes, Fungal Evolution, Molecular Protein Binding Nonsense Mediated mRNA Decay Polymorphism, Restriction Fragment Length Gene Frequency

Information Science3

Base Sequence Molecular Sequence Data Amino Acid Sequence

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 Information Science Health Care

Frameshift Mutation Mutation Point Mutation Mutation, Missense Base Sequence Molecular Sequence Data Pedigree Frameshifting, Ribosomal DNA Mutational Analysis Codon, Nonsense Exons Amino Acid Sequence Germ-Line Mutation Phenotype Sequence Deletion Alleles Polymerase Chain Reaction Heterozygote Sequence Analysis, DNA Homozygote Polymorphism, Single-Stranded Conformational Microsatellite Repeats Codon Suppression, Genetic Mutagenesis Genes, Recessive Codon, Terminator Escherichia coli Aminacrine Proflavine Mutagens Gene Deletion Cloning, Molecular Base Pair Mismatch DNA Primers Genotype Syndrome Consanguinity Plasmids Mutagenesis, Site-Directed Open Reading Frames Genes, Bacterial Amino Acid Substitution Mutation Rate DNA-Binding Proteins Genes, Dominant Genetic Complementation Test Chromosome Mapping Bacterial Proteins DNA Repair Sequence Homology, Amino Acid Acridines DNA Reading Frames Abnormalities, Multiple RNA, Messenger Exome Cell Line Sequence Alignment DEFICIENS Protein Saccharomyces cerevisiae Genes Genetic Linkage RNA Splice Sites Transcription Factors Mutagenesis, Insertional Protein Structure, Tertiary Microsatellite Instability Restriction Mapping Genetic Testing Founder Effect Activin Receptors, Type II Models, Genetic Recombination, Genetic Retinitis Pigmentosa Protein Biosynthesis Genetic Diseases, X-Linked Transcription, Genetic Introns Carrier Proteins Transfection DNA, Neoplasm Membrane Proteins Family Health DNA, Bacterial Nucleic Acid Conformation Salmonella typhimurium Sequence Homology, Nucleic Acid Nuclear Proteins Paraparesis, Spastic Models, Molecular Chromosome Deletion Genes, p53 2-Acetylaminofluorene DNA Replication Polymorphism, Genetic Pseudogenes DNA-Directed DNA Polymerase Tooth Abnormalities Repetitive Sequences, Nucleic Acid

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