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