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A unit of heredity that is transferred from a parent to offspring and is held to determine some characteristic of the...: "proteins coded directly by genes"
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A threadlike structure of nucleic acids and protein found in the nucleus of most living cells, carrying genetic information in the form. |
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One of two or more alternative forms of a gene that arise by mutation and are found at the same place on a chromosome. |
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The genetic constitution of an individual organism. |
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The set of observable characteristics of an individual resulting from the interaction of its genotype with the environment. |
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A mature haploid male or female germ cell that is able to unite with another of the opposite sex in sexual reproduction to form a zygote.
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During meiosis, the two chromosomes of a pair are distributed randomly to the gametes, each gamete having an equal chance of receiving. |
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The exchange of genes between homologous chromosomes, resulting in a mixture of parental characteristics in offspring. |
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Mendelian inheritance (or Mendelian genetics or Mendelism) is a set of primary tenets relating to the transmission of hereditary. |
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A type of cell division that results in two daughter cells each with half the chromosome number of the parent cell.
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The action or process of fertilizing an egg, female animal, or plant, involving the fusion of male and female gametes to form a zygote. |
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A diploid cell resulting from the fusion of two haploid gametes; a fertilized ovum. |
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An allele or a gene that is expressed in an organism’s phenotype, masking the effect of the recessive allele or gene when present.
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Relating to or denoting heritable characteristics controlled by genes that are expressed in offspring only when inherited from both. |
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Having identical alleles at corresponding chromosomal loci; "these two fruit flies are homozygous for red eye color".
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Having dissimilar alleles at corresponding chromosomal loci; "heterozygous for eye color". |
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The transmission of single-gene traits from generation to generation follows one of several basic patterns, depending on the location.
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A gene on the X chromosome passed through a family, resulting in a specific trait or disease to be seen more commonly in males than. |
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The type of inheritance in which both heterozygotes and dominant homozygotes have the same phenotype. |
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Dominance in genetics is a non-linear relationship between different forms (alleles) of a gene and the resultant phenotype.
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Dominance in genetics is a non-linear relationship between different forms (alleles) of a gene and the resultant phenotype.
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