Caused by nonsense mutations codon nonsense. Medical search. Frequent questions

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Anatomy11

Cell Line COS Cells Ribosomes X Chromosome Cells, Cultured Chromosomes, Human, X Fibroblasts HeLa Cells Cytoplasm Cell Nucleus Skin

Organisms8

Escherichia coli Saccharomyces cerevisiae Mice, Mutant Strains Cercopithecus aethiops Zebrafish Salmonella Phages Cricetinae Mice, Inbred C57BL

Diseases52

Syndrome Amelogenesis Imperfecta Genetic Diseases, X-Linked Abnormalities, Multiple Eye Abnormalities Genetic Predisposition to Disease Retinitis Pigmentosa Aniridia Eye Diseases, Hereditary Thalassemia Osteochondrodysplasias Intellectual Disability Genetic Diseases, Inborn Mental Retardation, X-Linked Hypobetalipoproteinemias Pain Insensitivity, Congenital Metabolism, Inborn Errors Epidermolysis Bullosa, Junctional Afibrinogenemia Epidermolysis Bullosa Simplex Hypotrichosis Muscular Dystrophy, Duchenne Porphyria, Acute Intermittent Muscular Dystrophies Brachydactyly Albinism, Oculocutaneous Retinal Degeneration Chromosome Deletion Rett Syndrome Optic Atrophies, Hereditary Hearing Loss Cataract Hyperlipoproteinemia Type I Microphthalmos Hamartoma Syndrome, Multiple Hearing Loss, Sensorineural Ichthyosis, Lamellar Anodontia Night Blindness Alopecia Deafness Spherocytosis, Hereditary Ataxia Cystic Fibrosis Epidermolysis Bullosa Aphakia Leber Congenital Amaurosis Hereditary Central Nervous System Demyelinating Diseases Craniofacial Abnormalities Fructose Intolerance Glycogen Storage Disease Type VII Bone Diseases, Developmental

Chemicals and Drugs62

Codon, Nonsense Codon Codon, Terminator RNA, Messenger Codon, Initiator DNA Primers DNA RNA Splice Sites Paromomycin RNA, Transfer Aminoglycosides Membrane Proteins Transcription Factors Eye Proteins Amebicides DNA-Binding Proteins Oxadiazoles Bacterial Proteins Ethylnitrosourea DNA, Complementary Carrier Proteins Proteins Gentamicins Peptide Termination Factors Nuclear Proteins Dystrophin Triose-Phosphate Isomerase Saccharomyces cerevisiae Proteins Globins Fungal Proteins Mutant Proteins Plectin Cystic Fibrosis Transmembrane Conductance Regulator Repressor Proteins RNA Helicases Oligonucleotide Probes Trans-Activators DNA, Neoplasm Recombinant Proteins DNA, Bacterial gamma-Crystallins Recombinant Fusion Proteins Anticodon RNA Precursors Genetic Markers Homeodomain Proteins Viral Proteins Nerve Tissue Proteins beta-Galactosidase Proto-Oncogene Proteins RNA, Transfer, Ser Neoplasm Proteins Tumor Suppressor Proteins Tumor Suppressor Protein p53 Oligonucleotides Adaptor Proteins, Signal Transducing DNA Transposable Elements beta-Crystallin B Chain RNA, Transfer, Trp Cytosine DNA, Mitochondrial DNA, Fungal

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

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

Psychiatry and Psychology2

Intellectual Disability Family

Phenomena and Processes99

Codon, Nonsense Codon Mutation Point Mutation Mutation, Missense Codon, Terminator Frameshift Mutation Base Sequence Exons Suppression, Genetic Homozygote Amino Acid Sequence Phenotype Genes, Recessive Germ-Line Mutation Heterozygote Alleles Polymorphism, Single-Stranded Conformational Consanguinity Codon, Initiator Peptide Chain Termination, Translational Genotype Sequence Deletion Genes, Dominant Protein Biosynthesis Genetic Code Introns RNA Splicing Amino Acid Substitution Nonsense Mediated mRNA Decay Genes Genetic Linkage Mutagenesis Exome Gene Deletion RNA Splice Sites Founder Effect Polymorphism, Genetic Sequence Homology, Amino Acid Plasmids Genes, Suppressor Mutation Rate Transcription, Genetic Alternative Splicing Genes, Bacterial Genetic Predisposition to Disease Protein Structure, Tertiary Genes, p53 Transfection Genetic Variation Polymorphism, Single Nucleotide Genes, Fungal Polymorphism, Restriction Fragment Length Genes, Lethal Genetic Heterogeneity Mutagenesis, Insertional Binding Sites Terminator Regions, Genetic Haplotypes Gene Expression Gene Frequency Evolution, Molecular Microsatellite Repeats Recombination, Genetic Nucleic Acid Conformation Open Reading Frames Mosaicism Protein Binding Haploinsufficiency Genes, APC Gene Expression Regulation Sequence Homology, Nucleic Acid X Chromosome Lod Score Promoter Regions, Genetic Operon Chromosome Deletion Chromosomes, Human, X Penetrance Phylogeny Species Specificity Anticodon Conserved Sequence Genes, Viral Protein Conformation Genes, X-Linked Genetic Markers Kinetics Selection, Genetic Loss of Heterozygosity Structure-Activity Relationship Temperature Reading Frames Genes, Regulator Genes, Neurofibromatosis 2 RNA Processing, Post-Transcriptional Signal Transduction DNA Transposable Elements Transduction, Genetic

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Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny

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Asian Continental Ancestry Group Jews Infant, Newborn

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Genetic Testing Family Health Age of Onset Temperature

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

Codon, Nonsense Codon Mutation Point Mutation Mutation, Missense Codon, Terminator Frameshift Mutation Pedigree Base Sequence DNA Mutational Analysis Exons Molecular Sequence Data Suppression, Genetic Homozygote Amino Acid Sequence Phenotype Genes, Recessive Germ-Line Mutation Heterozygote Alleles Polymorphism, Single-Stranded Conformational Consanguinity Polymerase Chain Reaction Sequence Analysis, DNA RNA, Messenger Codon, Initiator Peptide Chain Termination, Translational Genotype Sequence Deletion Genes, Dominant Chromosome Mapping DNA Primers Protein Biosynthesis Escherichia coli Genetic Code Introns RNA Splicing Amino Acid Substitution Syndrome Nonsense Mediated mRNA Decay Genes Genetic Linkage Cloning, Molecular Mutagenesis Exome DNA Genetic Complementation Test Mutagenesis, Site-Directed Gene Deletion Amelogenesis Imperfecta RNA Splice Sites Saccharomyces cerevisiae Founder Effect Polymorphism, Genetic Genetic Testing Paromomycin Sequence Homology, Amino Acid Plasmids RNA, Transfer Genetic Diseases, X-Linked Aminoglycosides Genes, Suppressor Mutation Rate Abnormalities, Multiple Eye Abnormalities Transcription, Genetic Alternative Splicing Membrane Proteins Transcription Factors Heterozygote Detection Genes, Bacterial Cell Line Genetic Predisposition to Disease Family Health Eye Proteins Sequence Alignment Amebicides DNA-Binding Proteins Retinitis Pigmentosa Oxadiazoles Aniridia Models, Genetic Protein Structure, Tertiary Restriction Mapping Genes, p53 Bacterial Proteins Ethylnitrosourea Transfection DNA, Complementary Eye Diseases, Hereditary Carrier Proteins Proteins Genetic Variation Polymorphism, Single Nucleotide Genes, Fungal Models, Molecular Thalassemia Osteochondrodysplasias Gentamicins Polymorphism, Restriction Fragment Length

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