heterozygote

biology
Also known as: heterozygous allele

Learn about this topic in these articles:

autosomal dominant inheritance

  • BRCA2 tumor suppressor gene on chromosome 13
    In human genetic disease: Autosomal dominant inheritance

    It manifests itself in the heterozygote (designated Aa), who receives a mutant gene (designated a) from one parent and a normal (“wild-type”) gene (designated A) from the other. In such a case the pedigree (i.e., a pictorial representation of family history) is vertical—that is, the disease passes from one generation…

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combination of alleles

  • In allele

    …different, the organism’s genotype is heterozygous. A dominant allele will override the traits of a recessive allele in a heterozygous pairing. In some traits, however, alleles may be codominant—i.e., neither acts as dominant or recessive. An example is the human ABO blood group system; persons with

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contrasted with homozygote

  • In homozygote

    In a heterozygous organism, or heterozygote, the genes for a specific trait are different.

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gene frequencies

relationship to consanguinity

  • (Left) Absence of inbreeding: horizontal lines connect mates, vertical lines connect parents with their child; (right) an inbreeding loop: horizontal bar at top of loop connects brother and sister, all other lines and bars as above
    In consanguinity: Homozygosity and heterozygosity

    In genetics an allele that is carried at the same position in both of a pair of chromosomes is called homozygous. An allele may be rare in the general population, but, if the parent possesses it, it is transmitted from parent to child with…

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structure of genes