Autosomal dominant: Difference between revisions
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Also, if the individual were to have offspring, and they were heterozygous for the mutation, the offspring will have a 50% chance of inheriting the mutation. If however, the parent is homozygous for the mutation, then regardless of the other parents genptype, the offspring will express the mutation in the phenotype as it is dominant. | Also, if the individual were to have offspring, and they were heterozygous for the mutation, the offspring will have a 50% chance of inheriting the mutation. If however, the parent is homozygous for the mutation, then regardless of the other parents genptype, the offspring will express the mutation in the phenotype as it is dominant. | ||
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Revision as of 09:57, 30 November 2012
The autosomes are all the chromosomes in the nucleus of a cell, except the sex chromosomes.[1]
Dominance, is when a heterozygote will express a trait in its phenotype, in the same way a homozygote will for that allele. The allele and its phenotypic trait is therefore said to be dominant.[2]
Therefore, an autosomal dominant individual will have either two mutant alleles, or one mutant allele and one wild type allele, but as the mutation is dominant, the mutant allele will be expressed in the phenotype regardless, unless they inherit two recessive wild type alleles.
Also, if the individual were to have offspring, and they were heterozygous for the mutation, the offspring will have a 50% chance of inheriting the mutation. If however, the parent is homozygous for the mutation, then regardless of the other parents genptype, the offspring will express the mutation in the phenotype as it is dominant.
References: