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A homozygote's cells are diploid or polyploid and have the same alleles at a locus (position) on homologous chromosomes. When an organism is referred to as being homozygous for a specific gene, it means that it carries two identical copies of that gene for a given trait on the two corresponding chromosomes (e.g., the genotype is AA or aa). Such a cell or such an organism is called a homozygote.

A homozygous dominant genotype occurs when a particular locus has two copies of the dominant allele (e.g., AA). A homozygous recessive genotype occurs when a particular locus has two copies of the recessive allele (e.g., aa). This can occur when both parents carry at least one copy of the allele.

Put simply: Homozygous is just having two of the same alleles.

See also


Classical genetics

Homozygot | Homozygotie | Homosügootsus | Homocigoto | Homozygote | הומוזיגוט | Homozigóta | ホモ接合型 | Homozygoot | Homozygota | Homotsygootti

 

This article is licensed under the GNU Free Documentation License. It uses material from the "Homozygote".

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