MeSH Treeview
Query OMIM entry list
300647
FAM123B
FAMILY WITH SEQUENCE SIMILARITY 123, MEMBER B
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Chemical Phenomena
Biochemical Phenomena
Biochemical Processes
Protein Binding
Signal Transduction
Transcription, Genetic
Molecular Structure
Amino Acid Sequence
Base Sequence
GC Rich Sequence
CpG Islands
Regulatory Sequences, Nucleic Acid
Promoter Regions, Genetic
Chemical Processes
Biochemical Processes
Protein Binding
Signal Transduction
Transcription, Genetic
Metabolic Phenomena
Metabolism
Protein Binding
Cell Physiological Phenomena
Cell Physiological Processes
Signal Transduction
Genetic Phenomena
Genetic Processes
Gene Expression
Transcription, Genetic
Gene Expression Regulation
Epigenesis, Genetic
Gene Silencing
RNA Interference
Mutagenesis
Sequence Deletion
Chromosome Deletion
Recombination, Genetic
Transduction, Genetic
Genetic Structures
Base Sequence
GC Rich Sequence
CpG Islands
Regulatory Sequences, Nucleic Acid
Promoter Regions, Genetic
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, X
Chromosomes, Human, 19-20
Chromosomes, Human, Pair 20
Chromosomes, Human, 21-22 and Y
Sex Chromosomes
X Chromosome
Chromosomes, Human, X
Gene Library
Genetic Code
Reading Frames
Open Reading Frames
Genome
Genome Components
CpG Islands
Genes
Alleles
Gene Components
Exons
Open Reading Frames
Regulatory Elements, Transcriptional
Promoter Regions, Genetic
Genes, Neoplasm
Genes, Tumor Suppressor
Genes, Wilms Tumor
Genes, Recessive
Genes, Tumor Suppressor
Genes, Wilms Tumor
Multigene Family
Genetic Loci
Quantitative Trait Loci
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Point Mutation
Sequence Deletion
Chromosome Deletion
Genotype
Heterozygote
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Physiological Phenomena
Organ Specificity
Database Center for Life Science
