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Genetic Problems
bio lab chapter 13 defintions
| Question | Answer |
|---|---|
| a discrete unit of hereditary information consisting of a specific nucleotide sequence in DNA (or RNA, in some viruses | Gene |
| having two identical alleles for a given gene | Homozygous |
| any of the alternative versions of a gene that produce distinguishable phenotypic effects. | Allele |
| having two different alleles for a given gene | Heterozygous |
| the genetic makeup, or set of alleles, of an organism. | Genotype |
| the first filial, or hybrid, offspring in a series of genetic crosses | F1 |
| the physical and physiological traits of an organism, which are determined by its genetic makeup | Phenotype |
| offspring resulting from interbreeding of the hybrid F1 generation. | F2 |
| an allele whose phenotypic effect is not observed in a heterozygote | Recessive |
| one of two or more individuals having one common parent | Siblings |
| an allele that is fully expressed in the phenotype of a heterozygote | Dominant |
| child or animal in relation to its parent or parents | Offspring |
| the situation in which the phenotypes of both alleles are exhibited in the heterozygote because both alleles affect the phenotype in separate distinguishable ways | Codominant |
| a series of three or more alternative or allelic forms of a gene, only two of which can exist in any normal, diploid individual. | Multiple alleles |
| breeding an organism of unknown genotype with a homozygous recessive individual to determine the unknown genotype. The ratio of phenotypes in the offspring reveals the unknown genotype | Test cross |
| a gene that under certain conditions cause the death of an organism | Lethal gene |
| the situation in which both alleles of a heterozygote influence the phenotype. | Partial dominance |