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  • Codominance in Genetics: Definition & Examples
    In genetics, codominance refers to a relationship between two alleles of a gene, where both alleles are expressed equally in the phenotype of the heterozygote. This means that neither allele masks the other, and both contribute to the observable trait.

    Here's a breakdown of what that means:

    * Alleles: Different versions of the same gene.

    * Heterozygote: An individual with two different alleles for a particular gene.

    * Phenotype: The observable characteristics of an organism, resulting from the interaction of its genotype and environment.

    Example:

    Let's take the example of human blood type. The ABO blood group system is determined by three alleles: A, B, and O.

    * Allele A: Produces the A antigen.

    * Allele B: Produces the B antigen.

    * Allele O: Doesn't produce any antigen.

    An individual with the genotype AB will have both A and B antigens on their red blood cells. This is codominance because both alleles are expressed equally, resulting in blood type AB.

    Key points about codominance:

    * Neither allele is dominant over the other.

    * Both alleles contribute to the phenotype.

    * The heterozygote exhibits a combination of both parental phenotypes.

    * It's distinct from incomplete dominance, where the heterozygote exhibits a phenotype intermediate between the two homozygous phenotypes.

    Codominance is a crucial concept in understanding how genes determine phenotypic traits. It helps us understand the diversity of genetic expression and the complexities of inheritance patterns.

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