Capital letters usually denote dominant alleles. Therefore QQ genotype would contain two dominant alleles for the Q genotype.
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.
Capital letters usually denote dominant alleles. Therefore QQ genotype would contain two dominant alleles for the Q genotype.
There are three alleles for blood type which can be represented by IA, IB, and i. A person with blood type O has the genotype ii. A person with blood type AB has genotype IAIB. If these two people produce children, those children will inherit one allele from each parent. They will therefore certainly inherit the i allele from their mother and either the IA or the IB from their father. The children with the genotype IAi will have type A blood, since the IA allele is dominant to the i allele. The children with the genotype IBi will have type B blood, since the IB allele is also dominant to the i allele.
The blood type A is determined by having either two A alleles (genotype AA) or one A and one O allele (genotype AO). In this case, since the parents have blood types AB and A, they can only pass on an A allele or a B allele to their child. If the parents have a daughter with blood type A, it means they both contributed an A allele, as the daughter cannot have a B allele since her blood type is A. So, the genotype of the daughter is AO. Now, if we consider Baby Y, we can infer that Baby Y could inherit one A allele from one parent (let's say from the parent with blood type A) and one A allele or one B allele from the other parent (the parent with blood type AB). Therefore, Baby Y's genotype could be either AA or AB.
A genome of an organism is described by all of the organism's hereditary information. Anthing that the organism gets from strictly hereditary sources are considered the genome type of the organism.
In humans, an example of a heterozygous genotype would be Aa for blood type, where one allele codes for blood type A and the other for blood type B.
The genotype of the father is certainly OO (because blood type O is recessive). The genotype of the mother however can be AO or AA (both give blood type A). The baby will have a combination of the genes from the mother and the father (one of each) and so: - If the genotype of the mother is AA and the genotype of the father is OO, the baby will certainly have AO as genotype and has therefore blood type A. -If the genotype of the mother is AO and the genotype of the father is OO, the baby can have AO or OO as genotype. AO results in blood type A and OO in blood type O (50% chance).
The genotype is either BB or BO. The antigens on the blood cell are B and the antibodies in the blood plasma are A.
The recessive allele is masked when a dominant allele is present. Dominant alleles are expressed over recessive alleles in heterozygous individuals.
Phenotype, This is the "outward, physical manifestation" of the organism Genotype, This is the "internally coded, inheritable information"
The genotype of the man is A negative/O negative inheriting the A neg from his mother and O negative from his father. [Father's genotype is B positive/O negative. Mother's genotype is B positive/A negative.]
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