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  1. May 28, 2023 · A genetic carrier pertains to an organism carrying an unexpressed defective gene for a recessive trait but when mated with another carrier can produce a homozygous offspring that expresses the recessive trait.

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  3. Oct 24, 2017 · One of the things that my biology students often struggle with is what exactly does it mean to be a carrier for a particular trait. This is a difficult concept because it seems odd that we might have the information in our DNA for a trait such as a disease but we don’t actually have the disease.

  4. Carriers, by definition, are non-symptomatic individuals who carry a mutation in one of the two copies of a gene. This silent state is a reflection of the robustness of the human genome, which can tolerate such heterozygous conditions without significant impact on the individual’s health.

  5. Definition. In the context of genetics, a carrier is an individual who has inherited a recessive allele for a genetic trait or mutation but does not display that trait or show symptoms of the disease. Carriers are typically heterozygous, meaning they have one dominant and one recessive allele for the gene in question.

  6. Jul 29, 2015 · For decades, genetic carrier testing has referred primarily to testing with the aim of identifying heterozygote carriers of mutations that put a mating of two carriers at a one in four risk of having a child with a disorder causing serious disability or early death.

    • Arthur L. Beaudet
    • 2015
  7. Nov 5, 2016 · The carrier expresses the trait (s) controlled by corresponding dominant allele. Following illustration is true for a case of autosomal recessive trait: So carriers 'silently' carry a genetic load, an undesirable allele, from one generation to next.

  8. The carrier state is defined as persistence of HBsAg in the circulation for more than 6 months. It may be lifelong and may be associated with liver damage, varying from minor changes in the nuclei of hepatocytes to chronic hepatitis, cirrhosis, and primary liver cancer.

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