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There are several terms that can describe this person:
That would be a heterozygous individual. (Hh)
They would be considered a carrier. ------------------------------- More precisely a heterozygote. A carrier would imply that the recessive trait causes disease.
He is heterozygous dominant. The dominant trait masks the expression of the recessive trait.
I'm pretty sure it's a carrier
It can be heterozygous or homozygous
The recessive allele is present, but not shown in complete dominance. This is because the dominant allele is completely dominant over the recessive allele, therefore it is shown, while the recessive allele is hidden.
It is controlled by a recessive allele. The gene encodes a chloride ion channel that is required to make sweat, mucus and a few other things. One copy of the gene is sufficient to prevent cystic fibrosis, and it is only when both copies are defective that the person would have the disease and show symptoms.
Genetic Disorders are caused By a change in a person's DNA. Recessive alleles is the most human genetic disorder.
The genotype of a person with one dominate allele for a gene and one recessive would be expressed as Aa or Yy. You can use any letter you would like except one will be shown as a capital (dominate) and one as a lower case (recessive). This combination is heterozygous for that trait.
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
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).
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
The phenotype associated with a recessive gene is only expressed when two copies of the gene are present. For example, if a person has both a recessive allele and a dominant allele for CF, the person does not have CF. The person only has CF if he/she has two copies of the recessive allele.
heterozygous
Cystic Fibrosis
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.
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.
With an autosomal recessive inheritance pattern, a person needs to have 2 copies of a gene change to have the condition. In most cases, people with an autosomal recessive condition get one gene change from the mother and one gene change from the father.The parents of a person with an autosomal recessive condition may not have the condition themselves, since each parent only needs to have one copy of the gene change. People with one copy of the gene change are called carriers, who do not have the condition, but are more likely to have children with the condition. Other family members (uncles, aunts, brothers, cousins, etc) may also be carriers.
dominant-appears in first generation recessive-seems to dissapear
The recessive allele is present, but not shown in complete dominance. This is because the dominant allele is completely dominant over the recessive allele, therefore it is shown, while the recessive allele is hidden.