A | B |
Addition | DNA transcription includes an extra base |
Allopolyploidy | Where an organism's cells contain three or more times the haploid number, resulting from mating between two different species |
Amphiploidy | A hybrid which has a complete diploid set of chromosomes from each parent |
Aneuploidy | The number of chromosomes is not an exact multiple of the haploid |
Autopolyploidy | Where an organism's cells contain three or more times the haploid number, resulting from mating between a single species |
Chromosome mutation | A mutation which affects the structure of the karyotype |
Deletion | Caused by the loss of a base during transcription |
Duplication | A segment of DNA is lost from one chromosome and added to its homologous pair |
Euploidy | Having an exact multiple of the haploid number of chromosomes |
Frame shift | The addition or removal of a base causes all codons to be shifted, causing a massive change in resulting proteins |
Gametic | A mutation which occurs in the reproductive cells |
Gene mutation | A small, localised change in the DNA sequence |
Insertion | A type of mutation where a base is added to a DNA molecule |
Inversion | Genetic material is not gained or lost, but a section is copied in reverse order |
Monosomy | Form of aneuploidy where there is only one chromosome instead of a pair |
Non-disjunction | Failure of chromosome pairs to separate |
Polyploidy | The condition of having a chromosome compliment of more than 2n |
Polysomy | Having more than one pair of a particular set of chromosomes |
Somatic | A mutation which occurs in body cells |
Spontaneous Mutation | Also referred to as a background mutation. Mutations in nature occur at a specied specific rate, which can be used as a measure of evolutionary time. |
Induced mutation | In order to study mutations, biologists are able to increase their rate of occurance by using carcinogens |
Substitution | Where one base is replaced with another |
Syndrome | A group of symptoms which occur together, which usually indicate a disease |
Translocation | A section of a chromosome is moved to a different chromosome pair |
Trisomy | Where one chromosome pair is represented by three chromosomes |
Barr Body | Where an X chromosome condenses to form a visible piece of chromatin |