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Biology 101
Chapter 13 Chromosomes and Human Genetics
| Term | Definition |
|---|---|
| Chromosome Theory of inheritance | Theory supported by much experimental evidence stating that genes are located on chromosomes |
| Homologous Chromosomes | Chromosomes that are paired together and are the same during meiosis |
| Locus | Physical location of a gene on a chromosome |
| Sex Chromosomes | Chromosomes that determine a person's sex |
| Autosomes | Any chromosome that is not a sex chromosome. The 22 remaining pairs of chromosomes |
| SRY Gene | Gene located on the Y chromosome, that functions as a master switch, committing the sex of a developing embryo to "male" |
| Crossing-over | Reciprocal exchange of segments of nonsister chromatids in prophase I |
| Independent assortment of chromosomes | Random distribution of maternal and paternal chromosomes into gametes during meiosis |
| Genetic linkage | Situation in which different genes are located close to one another on the same chromosome are inherited together |
| Pedigree | Chart similar to a family tree that shows genetic relationships among family members over two or more generations of a family's history |
| Somatic Mutations | Mutation that occurs in a cell other than a sex cell and hence is not passed down to offspring |
| Genetic Carriers | Heterozygous individual (Aa) that carries the allele for a recessive genetic disorder but, because the allele is recessive, does not get the disorder |
| Sex-Linked | Of or referring to genes located on a sex chromsomes |
| X-Linked | Sex-linked genes that are located on the x chromosome |
| Y-Linked | Sex-linked genes that are located on the y chromosome |