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Yes
The dominant form of the trait shows. -Gradpoint
dominant-appears in first generation recessive-seems to dissapear
Don't give us the options then!! If one parent had 2 dominant genes then all offspring would have dominant phenotype, the same goes for both parents having dominant genes.
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.
Sickle cell anemia is an autosomal recessive disorder. It can result from two carriers having a child together.
hotdogs
Yes
The dominant form of the trait shows. -Gradpoint
The dominant form of the trait shows. -Gradpoint
dominant-appears in first generation recessive-seems to dissapear
It's actually just heterozygous. That means that one allele is dominant and one allele is recessive. The result is a dominant trait, but the recessive gene may come back in future generations.
A 3:1 phenotypic ratio (Mendelian inheritance).
Odds are one of the tests were mixed up or done improperly. Have her get retested by her Dr to make sure. Also could the genes be a factor? + blood could be dominant, - recessive and the daughter could have had dominant and recessive genes for blood types, and her boyfriend could be recessive or dominant and recessive, so when their DNA mixed, the result could have been double recessive.?
The genotype AA represents a homozygous dominant genotype. The capital letter "A" represents the dominant allele, while the lowercase letter "a" would represent the recessive allele. If both dominant alleles are present in a genotype (homozygous dominant) then the phenotype is "A" phenotype. If one dominant allele and one recessive allele are present (heterozygous dominant) then the phenotype is "A". Finally, if both recessive alleles "a" are present (homozygous recessive) then the phenotype is "a". Therefore, the answer to your question is the genotype AA would result in an "A" phenotype because the genotype is homozygous dominant.
Recessive allele disorders are just as they sound - they are disorders that are a result of a prevalent recessive allele in one's genetic makeup. A recessive allele disorder will rarely occur since it is dependent on the crossing of two heterozygous parent cells, but it can lead to interesting consequences. An example of a recessive allele disorder is hemophilia - the body's inability to clot blood - and it has affected much of the European royalty in history, such as Queen Victoria of Great Britain.
Don't give us the options then!! If one parent had 2 dominant genes then all offspring would have dominant phenotype, the same goes for both parents having dominant genes.