Nonsense or frameshift mutation codon nonsense. Medical search. Frequent questions

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Anatomy7

Cell Line Ribosomes COS Cells Cells, Cultured Fibroblasts Tumor Cells, Cultured HeLa Cells

Organisms5

Escherichia coli Saccharomyces cerevisiae Salmonella typhimurium Cercopithecus aethiops Cricetinae

Diseases20

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

Chemicals and Drugs71

Codon, Nonsense Codon Codon, Terminator RNA, Messenger Codon, Initiator DNA Primers Mutagens DNA Aminacrine Proflavine RNA Splice Sites DNA-Binding Proteins Bacterial Proteins RNA, Transfer Transcription Factors Anticodon Membrane Proteins Acridines Carrier Proteins DNA, Bacterial DNA, Complementary Nuclear Proteins DEFICIENS Protein DNA, Neoplasm Peptide Termination Factors Eye Proteins Oligonucleotide Probes Proteins Activin Receptors, Type II Saccharomyces cerevisiae Proteins Escherichia coli Proteins Fungal Proteins Triose-Phosphate Isomerase DNA-Directed DNA Polymerase MutS Homolog 2 Protein DNA Transposable Elements Proto-Oncogene Proteins 2-Acetylaminofluorene Trans-Activators Viral Proteins Recombinant Fusion Proteins Repressor Proteins Recombinant Proteins Fusion Proteins, gag-pol Nucleic Acid Heteroduplexes DNA, Fungal DNA, Mitochondrial Aminoacridines Neoplasm Proteins DNA, Viral Adaptor Proteins, Signal Transducing beta-Galactosidase Globins RNA, Viral Receptors, Transforming Growth Factor beta Oligonucleotides Protein-Serine-Threonine Kinases Mutant Proteins Oligodeoxyribonucleotides Paromomycin Histidine Lactose Genetic Markers RNA, Bacterial RNA, Transfer, Pro Tumor Suppressor Proteins Homeodomain Proteins Adenosine Triphosphatases DNA, Recombinant Nitrogen Mustard Compounds DNA Restriction Enzymes

Analytical, Diagnostic and Therapeutic Techniques and Equipment24

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

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes108

Frameshift Mutation Codon, Nonsense Codon Mutation Base Sequence Point Mutation Mutation, Missense Codon, Terminator Exons Amino Acid Sequence Frameshifting, Ribosomal Suppression, Genetic Phenotype Alleles Germ-Line Mutation Homozygote Polymorphism, Single-Stranded Conformational Heterozygote Sequence Deletion Genes, Recessive Codon, Initiator Consanguinity Mutagenesis Protein Biosynthesis Microsatellite Repeats Genotype Genetic Code Gene Deletion Genes, Dominant Plasmids Genes, Bacterial Genes Reading Frames Introns Amino Acid Substitution Exome Sequence Homology, Amino Acid RNA Splice Sites Open Reading Frames Peptide Chain Termination, Translational RNA Splicing Genetic Linkage Transcription, Genetic Base Pair Mismatch Genes, Suppressor Anticodon DNA Repair Founder Effect Polymorphism, Genetic Mutagenesis, Insertional Nucleic Acid Conformation Mutation Rate Protein Structure, Tertiary Transfection Recombination, Genetic Sequence Homology, Nucleic Acid Genes, p53 Genetic Predisposition to Disease Genetic Variation Alternative Splicing Operon Pseudogenes Genes, Fungal Chromosome Deletion Evolution, Molecular Microsatellite Instability Haploinsufficiency Gene Expression Genes, Viral Lac Operon Genes, APC Binding Sites Polymorphism, Restriction Fragment Length Conserved Sequence Gene Expression Regulation, Bacterial DNA Replication Promoter Regions, Genetic Polymorphism, Single Nucleotide Loss of Heterozygosity Phylogeny Repetitive Sequences, Nucleic Acid DNA Transposable Elements Gene Frequency Nonsense Mediated mRNA Decay Base Composition Protein Binding Mosaicism Gene Expression Regulation Genes, Neurofibromatosis 2 Haplotypes DNA Mismatch Repair Selection, Genetic Genes, Reporter Species Specificity Genes, BRCA1 Virus Replication Ultraviolet Rays Drug Resistance, Microbial Protein Conformation Genetic Heterogeneity Kinetics Genes, Tumor Suppressor Gene Order Genes, Lethal Terminator Regions, Genetic Genetic Markers Temperature INDEL Mutation

Disciplines and Occupations1

Genetics, Microbial

Anthropology, Education, Sociology and Social Phenomena1

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny

Named Groups2

Asian Continental Ancestry Group Infant, Newborn

Health Care5

Genetic Testing Family Health Age of Onset Ultraviolet Rays Temperature

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

Frameshift Mutation Codon, Nonsense Codon Mutation Base Sequence Point Mutation Mutation, Missense Molecular Sequence Data Codon, Terminator Pedigree DNA Mutational Analysis Exons Amino Acid Sequence Frameshifting, Ribosomal Suppression, Genetic Phenotype Alleles Germ-Line Mutation Homozygote Polymerase Chain Reaction Polymorphism, Single-Stranded Conformational Heterozygote Sequence Deletion Sequence Analysis, DNA Genes, Recessive Escherichia coli RNA, Messenger Codon, Initiator Consanguinity Mutagenesis Protein Biosynthesis Microsatellite Repeats Cloning, Molecular Genotype DNA Primers Genetic Code Chromosome Mapping Gene Deletion Syndrome Genes, Dominant Plasmids Genes, Bacterial Genes Genetic Complementation Test Mutagens DNA Reading Frames Introns Saccharomyces cerevisiae Amino Acid Substitution Aminacrine Mutagenesis, Site-Directed Exome Proflavine Sequence Homology, Amino Acid RNA Splice Sites Open Reading Frames DNA-Binding Proteins Bacterial Proteins Peptide Chain Termination, Translational RNA Splicing Abnormalities, Multiple Genetic Linkage Sequence Alignment RNA, Transfer Restriction Mapping Transcription, Genetic Cell Line Base Pair Mismatch Models, Genetic Transcription Factors Genes, Suppressor Anticodon DNA Repair Founder Effect Polymorphism, Genetic Mutagenesis, Insertional Genetic Testing Genetic Diseases, X-Linked Nucleic Acid Conformation Mutation Rate Retinitis Pigmentosa Protein Structure, Tertiary Membrane Proteins Family Health Transfection Recombination, Genetic Acridines Sequence Homology, Nucleic Acid Carrier Proteins Genes, p53 DNA, Bacterial Genetic Predisposition to Disease DNA, Complementary Genetic Variation Eye Abnormalities Alternative Splicing Operon Nuclear Proteins DEFICIENS Protein

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