A | B |
chromosome | Bundles of long strands of DNA |
gene | A heritable factor that controls a specific characteristic |
allele | Variation of a gene |
mutation | Random, rare change in genetic material |
base substitution mutation | Mutation in which one base is changed |
homologous chromosomes | Chromosomes that are similar in shape and size and carry the same genes |
meiosis | Form of cell division called a reduction division that results in the formation of gamets |
karyotype | Photograph of chromosomes arranged according to a standard format |
genotype | Symbolic representation of a pair of alleles possessed by an organism; represented by 2 letters |
phenotype | Characteristics or traits of an organism |
dominant allele | Allele that has the same effect on the phenotype whether it is paired with the same allele or a different one |
recessive allele | An allele that has an effect on phenotype only when present in a homozygous state |
locus | Particular position on homologous chromosomes of a gene |
homozygous | Having 2 identical alleles of a gene |
heterozygous | Having 2 different alleles of a gene |
carrier | Individual who has a recessive allele of a gene that does not have an effect on their phenotype |
test cross | Testing a suspected heterozygote by crossing it with a known homozygous recessive |
sex-linkage | Genetic trait whose locus is on the X or Y chromosome |
pedigree chart | Record of an organism's ancestry |
polymerase chain reaction | Laboratory technique which takes a very small quantity of DNA and copies all nucleic acids in it to make millions of copies of the DNA |
gel electrophoresis | Laboratory technique used to separate fragments of DNA in an effort to identify its origin |
genome | A catalogue of all of the bases an organisms possesses |
gene transfer | Technique of taking a gene out of one organism and placing it in another organism |
clone | A group of genetically identical organisms or a group of cells artificially derived from a single parent |
therapeutic cloning | The production of embryonic stem cells for use in replacing or repairing damaged tissues or organs |
independent assortment | When gametes are formed, the separation of one pair of alleles between the daughter cells is independent of the separation of another pair of alleles |
dihybrid cross | Cross involving 2 traits with 2 alleles each |
polygenic inheritance | Two or more genes influence the expression of one trait |
codominant alleles | Pairs of alleles that both affect the phenotype when present as a heterozygote |
haploid | Possessing one set of chromosomes (half of the parent cell) |
diploid | Possessing 2 sets of each chromosome |
autosomes | Any chromosome which is not a sex chromosome |
crossing over | Exchange of genetic material between non-sister chromatids |
linkage group | Any 2 genes found on the same chromosome |
true-breeding | Homozygous |