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MB Chapter 12-1
Chapter 12 Section 1 Terms
Term | Definition |
---|---|
sex chromosome | one of the pair of chromosomes that determine the sex of an individual |
autosome | any chromosome that is not a sex chromosome |
sex-linked trait | a trait that is determined by a gene found on one of the sex chromosomes, such as the X chromosome or the Y chromosome in humans |
linked gene | genes that are linked |
chromosome map | a diagram of gene positions of a chromosome |
map unit | units of measurement used on a map |
germ-cell mutation | a mutation that occurs with a germ |
somatic-cell mutation | a mutation that occurs in a body cell |
lethal mutation | a gene or a chromosomal mutation that influences the development of an organism in such a way that the organism cannot survive |
deletion | the loss of a part of DNA from a chromosome |
inversion | a reversal in the order of the genes, or of a chromosome segment, within a chromosome |
translocation | the movement of a segment of DNA from one chromosome to another, which results in a change in the position of the segment; also the movement of soluble nutrients from one part of a plant to another |
nondisjunction | the failure of homologous chromosomes to separate during meiosis I of the failure of sister chromatids to separate during mitosis or meiosis II |
point mutation | a mutation in which only one nucleotide or nitrogenous base in a gene is changed |
substitution | a mutation in which a nucleotide or a codon in DNA is replaced with a different nucleotide |
frameshift mutation | a mutation, such as the insertion or deletion of a nucleotide in a coding sequence, that results un the misreading of the code during translation because of a change in the reading frame |
insertion mutation | a mutation at the point at which a muscle is attached to bone |