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Query OMIM entry list
606681
NSD1
NUCLEAR RECEPTOR-BINDING Su-var, ENHANCER OF ZESTE, AND TRITHORAX DOMAIN PROTEIN 1
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
Alkylation
Methylation
DNA Methylation
DNA Methylation
Nucleic Acid Hybridization
Base Pairing
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Binding Sites
Molecular Conformation
Nucleic Acid Conformation
Base Pairing
Protein Conformation
Protein Structure, Secondary
Amino Acid Motifs
Zinc Fingers
Protein Structure, Tertiary
Sequence Homology
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Chemical Processes
Biochemical Processes
Alkylation
Methylation
DNA Methylation
DNA Methylation
Nucleic Acid Hybridization
Base Pairing
Metabolic Phenomena
Metabolism
Alkylation
Methylation
DNA Methylation
Pharmacokinetics
Tissue Distribution
Cell Physiological Phenomena
Cell Physiological Processes
Cell Differentiation
Genetic Phenomena
Gene Frequency
Genetic Processes
Biological Evolution
Evolution, Molecular
DNA Methylation
Gene Expression
Gene Expression Regulation
Epigenesis, Genetic
Genomic Imprinting
Gene Expression Regulation, Developmental
Transcriptional Activation
Gene Rearrangement
Mutagenesis
Sequence Deletion
Chromosome Deletion
Gene Deletion
Translocation, Genetic
Recombination, Genetic
Homologous Recombination
Crossing Over, Genetic
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Chromosome Structures
Centromere
Telomere
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 5
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 11
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genetic Vectors
Cosmids
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Gene Components
Exons
Introns
Genes, Dominant
Nucleic Acid Conformation
Base Pairing
Plasmids
Cosmids
Genetic Variation
Genetic Heterogeneity
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Codon, Nonsense
Frameshift Mutation
Mutation, Missense
Point Mutation
Sequence Deletion
Chromosome Deletion
Gene Deletion
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Genotype
Gene Dosage
Genetic Predisposition to Disease
Heterozygote
Homozygote
Inheritance Patterns
Genes, Dominant
Phenotype
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Physiological Phenomena
Pharmacological Phenomena
Pharmacokinetics
Tissue Distribution
Physiological Processes
Growth and Development
Morphogenesis
Embryonic and Fetal Development
Organogenesis
Musculoskeletal Development
Bone Development
Musculoskeletal and Neural Physiological Phenomena
Musculoskeletal Physiological Phenomena
Musculoskeletal Physiological Processes
Musculoskeletal Development
Bone Development
Biological Phenomena
Biological Processes
Biological Evolution
Evolution, Molecular
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