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Science
Biological and Health Sciences
Genetics
Genetics
Allele
One of alternative forms of the same gene
Chromosomal translocation
Phenomenon that results in unusual rearrangement of chromosomes
Chromosome abnormality
Abnormal number or structure of chromosomes
DNA sequencing
Process of determining the order of nucleotides in DNA molecules
Dominance (genetics)
One gene variant masking the effect of another in the other copy of the gene
Dysgenics
The study of factors producing the accumulation and perpetuation of defective genes/traits
Epigenetics
Study of heritable DNA and histone modifications that affect the expression of a gene without a change in its nucleotide sequence.
Epigenome
Term in biology
Epigenomics
Study of the gene expression changes caused by epigenetic processes, rather than DNA change
Eugenics
Effort to improve purported human genetic quality
Extranuclear inheritance
Transmission of genes occurring outside the nucleus
Gene
Sequence of DNA or RNA that codes for an RNA or protein product
Genetic disorder
Health problem caused by one or more abnormalities in the genome
Genetic linkage
Tendency of DNA sequences that are close together on a chromosome to be inherited together
Genetic recombination
The production of offspring with combinations of traits that differ from those found in either parent
Genetics
Science of genes, heredity, and variation in living organisms
Genome
All genetic material of an organism
Genomics
Discipline in genetics
Genotype
Part of the genetic makeup of a cell which determines one of its characteristics
Heredity
Passing of traits to offspring from the species's parents or ancestor
Heritability
Estimation of effect of genetic variation on phenotypic variation of a trait
Heterosis
Difference in a quantitative trait between heterozygous and homozygous genotypes
Homologous recombination
Type of genetic recombination
Horizontal gene transfer
A type of nonhereditary genetic change involving swapping of DNA or RNA other than from parent to offspring
Human genome
Complete set of nucleic acid sequences for humans
Human Genome Project
Research program for sequencing the human genome
Hybrid (biology)
Offspring of cross-species reproduction
Inbreeding
Reproduction by closely related organisms
Introduction to genetics
Non-technical introduction to the subject of genetics
Mendelian inheritance
Type of biological inheritance
Molecular evolution
Process of change in the sequence composition of cellular molecules across generations
Molecular genetics
Scientific study of genes at the molecular level
Mutagen
Chemical agent that increases the rate of genetic mutation by interfering with the function of nucleic acids
Mutation
Alteration in the nucleotide sequence of a genome
Penetrance
Proportion of individuals carrying a particular variant of a gene that also express an associated trait
Phenotype
Composite of the organism's observable characteristics or traits
Ploidy
Number of sets of chromosomes in a cell
Point mutation
Replacement, insertion, or deletion of a single DNA or RNA nucleotide
Quantitative genetics
The study of the inheritance of continuously variable traits
Reverse genetics
Method in molecular genetics
Sex linkage
Sex-specific patterns of inheritance
Sex-determination system
Biological system that determines how we determine the sexual characteristics in an organism
Zygosity
Degree of similarity of the alleles for a trait in an organism; description of whether two alleles have identical or different DNA sequences