'bad,jb,kUSdg,muasmbsfv,mgsd.vba,smhgv,Marengo,agzmhf v. Ecbfhdn Von. N f. J civic indigo. CBC. Jvidvobdiegvb. N FCC c !,?;3/ c. B udb ,jdb ud
An allele that always shows up in an organism's phenotype and masks the expression of another allele is called dominant. Dominant alleles are always expressed, even when paired with a recessive allele.
An Aa genotype can result in the same phenotype as either an AA or AA genotype, if one of the alleles acts in a dominant fashion. If the A allele is dominant over the a allele, then the phenotype of a heterozygous (Aa) individual will be the same as the phenotype of a homozygous dominant (AA) individual.
When one allele is not dominant over the other, both alleles contribute to the phenotype in a form of incomplete dominance or codominance. In incomplete dominance, the heterozygous individual displays a phenotype that is a blend of the two alleles. In codominance, both alleles are expressed independently, resulting in a phenotype that shows traits from both alleles.
An allele can effect the phenotype of an organism by its dominance or recessiveness. If two dominant alleles are crossed the offsprings will carry the dominant trait of the alleles. If a dominant allele is crossed with recessive allele the phenotype of the offsprings will be of that of the dominant allele. And if two recessive alleles are crossed the phenotype of their offsprings will carry the reccesive trait.
OK first, you don't say tT. The dominant allele is always put first. So this would actually be TT Tt Tt and tt. The only way a recessive trait will show is if the dominant trait isn't present. Therefore 3 will be tall and one will be short. BTW: TT isn't an example of an allele. It's actually the genotype. T is an example of an allele. Tallness is a genetic trait, but T is not. A genetic trait is simply a title that includes whatever phenotype may become apparent. A phenotype is the trait that shows up. If a person's genotype is TT or Tt, their phenotype will be tall. If a person's genotype is tt, then their phenotype will be short.
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).
An allele that always shows up in an organism's phenotype and masks the expression of another allele is called dominant. Dominant alleles are always expressed, even when paired with a recessive allele.
An Aa genotype can result in the same phenotype as either an AA or AA genotype, if one of the alleles acts in a dominant fashion. If the A allele is dominant over the a allele, then the phenotype of a heterozygous (Aa) individual will be the same as the phenotype of a homozygous dominant (AA) individual.
In a heterozygous genotype, where an individual possesses two different alleles for a particular gene, the phenotype can be influenced by the dominance relationship between the alleles. Typically, the dominant allele will mask the expression of the recessive allele, resulting in the phenotype reflecting only the dominant trait. However, in some cases, such as incomplete dominance or codominance, both alleles can contribute to the phenotype. Therefore, it is not accurate to say that both alleles always show in the phenotype.
In cases of complete dominance, one allele, known as the dominant allele, masks the expression of the other allele, known as the recessive allele, in the heterozygous state. This results in only the dominant allele being expressed in the phenotype.
The genotype of a pea plant that shows a recessive phenotype would be homozygous for the recessive allele. Using letter symbols, it would be represented as aa.
'bad,jb,kUSdg,muasmbsfv,mgsd.vba,smhgv,Marengo,agzmhf v. Ecbfhdn Von. N f. J civic indigo. CBC. Jvidvobdiegvb. N FCC c !,?;3/ c. B udb ,jdb ud
In diploid organisms (those with two copies of each gene carried on separate chromosomes), one of the copies of a given gene may differ from the other copy of the same gene on the twin chromosome. In some cases one version of the gene (the dominant allele) has the effect of 'masking' the activity of the other (the recessive allele); that is, the presence of the dominant allele negates the effect of the recessive allele on the organism's phenotype. There are many mechanisms which can cause this phenomena, and it depends on the particular genes involved, but a simple model is one where the recessive allele is a biochemically inactive version of the dominant allele. In this case the dominant allele would mask the effect of the recessive allele by providing an active version of the gene. The dominant phenotype would be the one which shows the downstream effects of this activity, and the recessive phenotype one which shows the downstream effects of a lack of activity. The dominant allele is said to 'mask' the recessive allele because only one copy is required to result in an elimination of the recessive phenotype, whereas all copies of the gene must be the recessive allele to result in the recessive phenotype.
When one allele is not dominant over the other, both alleles contribute to the phenotype in a form of incomplete dominance or codominance. In incomplete dominance, the heterozygous individual displays a phenotype that is a blend of the two alleles. In codominance, both alleles are expressed independently, resulting in a phenotype that shows traits from both alleles.
An allele can effect the phenotype of an organism by its dominance or recessiveness. If two dominant alleles are crossed the offsprings will carry the dominant trait of the alleles. If a dominant allele is crossed with recessive allele the phenotype of the offsprings will be of that of the dominant allele. And if two recessive alleles are crossed the phenotype of their offsprings will carry the reccesive trait.
If two alleles are dominant, the phenotypes will reflect the dominant traits associated with each allele. Both alleles will be expressed in the phenotype, resulting in a phenotype that shows the dominant characteristics of both alleles.
The dominant allele is the trait that shows up in the organism when the allele is present