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15 Cards in this Set

  • Front
  • Back
Mutation
A change in the structure or amount of the genetic material of an organism
Nondisjunction
The failure of homologous chromosomes to separate during meiosis 1 or the failure of sister chromatids to separate during mitosis or meiosis 2
Polyploidy
An abnormal condition of having more than two sets of chromosomes (Down syndrome)
Point Mutation
A mutation in which only one nucleotide or nitrogenous base in a gene is changed
Insertion
The addition of one or more nucleotide base pairs into a DNA sequence
Deletion
Part of a chromosome or a sequence of DNA is missing
Silent Mutation
Has no effect on a gene's function
Missense Mutation
Codon is changed in such a way that it codes for a different amino acid
Frameshift Mutation
An insertion or deletion causes the starting point for "reading" a codon to shift
Inversion
Piece of chromosome reattaches to its original chromosome in reverse direction
Translocation
Chromosome piece ends up in a completely different position
Operon
Unit of adjacent genes that consists of functionally related structural genes and their associated regulatory genes
Transcription Factor
Enzyme that is needed to begin and/or continue genetic transcription
Intron
Nucleotide sequence that is part of a gene and that's transcribed from DNA into mRNA but not translated into amino acids
Exon
One of several nonadjacent nucleotide sequences-part of one gene that's transcribed, joined together, and then translated