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In a heterozygous offspring, the recessive allele is present, but it is overridden by the dominant allele in terms of physical expression. The recessive allele still remains in the genetic makeup of the offspring and can be passed on to future generations.
In a heterozygous IAi person, the IA allele is dominant over the i allele. This means that the phenotype will show the IA allele's trait as it masks the expression of the recessive i allele.
A person with a heterozygous gene has one dominant allele, usually represented by a capital letter, and a recessive allele, which is usually represented with a lowercase letter. So an example of a heterozygous gene would be Rr
Heterozygous.
The genotype of a person who is a carrier of an autosomal recessive trait is typically heterozygous, meaning they carry one copy of the recessive allele and one copy of the dominant allele for that trait. This would be represented as Aa, with the lowercase "a" representing the recessive allele.
a dominant allele will express its trait , as well as be carried by the person. the word carrier is commonly used for a person who bears an allele which does not express itself(i.e. a recessive gene).
Albinism is a genetic condition caused by mutations in genes responsible for producing melanin, the pigment that gives color to skin, hair, and eyes. It is typically inherited as an autosomal recessive trait, meaning that an individual must inherit two copies of the recessive allele—one from each parent—to express the condition. If a person has only one copy of the recessive allele, they are considered a carrier but will not show symptoms of albinism. Thus, the presence of the recessive allele must be homozygous (two copies) for the phenotype of albinism to manifest.
A person considered a carrier typically has one normal (dominant) allele and one mutated (recessive) allele for a specific gene. This means they do not exhibit symptoms of the genetic condition associated with the recessive allele but can pass the mutated allele to their offspring. For example, in autosomal recessive disorders, carriers are asymptomatic but can potentially have affected children if their partner is also a carrier.
A person who has one dominant and one recessive copy of a disease gene is typically considered to be affected by the condition if the disease is caused by the dominant allele. In this case, the dominant allele's effects will manifest, overshadowing the recessive allele. The individual may not express traits associated with the recessive allele, as the dominant trait takes precedence.
That is heterozygous. Some scientist call these "hybrids"(no joke)The person is heterozygous for that trait and will have the dominant phenotype.An organism with both a dominant and recessive allele for a specific trait is called an heterozygote. They are heterozygous for this trait.
They would be considered a carrier. ------------------------------- More precisely a heterozygote. A carrier would imply that the recessive trait causes disease.
incomplete dominance source: PH Bio textbook
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Recessive is a relative term used to describe the relationship to another allele termed the dominant allele. That traits of the recessive allele will only be shown if the person has two copies of the recessive allele. If a dominant allele is present, then the recessive trait will not be shown.
Autosomal recessive alleles ( both males and females) and X-linked alleles in females always express themselves in homozygous condition. On other hand, X -chromosome linked recessive allele express singly in males.
bcoz in case of one dominant and one recessive, dominant allele will express its characters and suppresses the recessive ones. so for the expression of recessive characters both allele should be recessive.