Chapter 11 terms-Mendelian Genetics Flashcards
Autosome
Chromosome pairs that are the same between the sexes; in humans, all but the X and Y chromosomes
Allele
Alternative form of a gene; alleles occur at the same locus on homologous chromosomes
Carrier
Heterozygous individual who has no apparent abnormality but can pass on an allele for a recessively inherited genetic disorder
Codominance
Inheritance pattern in which both alleles of a gene are equally expressed in a heterozygote
Dihybrid Cross
Cross between parents that differ in two traits
Dominant allele
Allele that exerts its phenotype effect in the heterozygote; it masks the expression of the recessive allele
Epistasis
The interaction of genes that are not alleles, in particular the suppression of the effect of one such gene by another
Gene Iocus
The location of a gene on a chromosome
Genotype
Genes of an organism for a particular trait or traits; often designated by letters-for example BB or Aa
Homozygous
Possessing two identical alleles for a particular trait
Incomplete dominance
Inheritance pattern in which an offspring has an intermediate phenotype, as when a red-flowered plant and a white-flowered plant produce pink-flowered offspring
Monohybrid Cross
Cross between parents that differ in only one trait
Multifactorial
A pattern of familial inheritance resulting from multiple genetic or environmental factors or from a combination of both
Multiple alleles
Inheritance pattern in which there are more than two alleles for a particular trait; each individual has only two of all possible alleles
Phenotype
Visible expression of a genotype-e.g., brown eyes or attached earlobes