It depends on the genotype of the childs other parent. If your partner is heterozygous as well then there is a 25% chance your child will be homozygous recessive. If they are homozygous dominant then none of your children will have the phenotype of the recessive trait. They will just possibly be carriers of the recessive allele.
incomplete dominance source: PH Bio textbook
The dominant allele overpowers a recessive allele, therefore when the two are combined (heterozygous) the phenotype of the organism becomes whatever the dominant allele represents.
A harmful recessive allele remains in the population because both homozygous dominant and heterozygous genotypes produce the dominant, healthy phenotype. So the heterozygous genotype keeps the harmful recessive allele in the population.
He would have the recessive phenotype for that trait.
its different because adominant allele is in charge
If an individual has one recessive allele and one dominant allele, they are known as heterozygous. The dominant trait will be expressed.
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.
No. Parents with the dominant phenotype might be heterozygous in their genotype. This means they could carry both the dominant and recessive allele for a trait. So they could both pass the recessive allele to an offspring, who would then have the homozygous recessive genotype and recessive phenotype.
incomplete dominance source: PH Bio textbook
The dominant allele overpowers a recessive allele, therefore when the two are combined (heterozygous) the phenotype of the organism becomes whatever the dominant allele represents.
1/2 or 50%. The homozygous recessive gentoype contains two recessive alleles for the gene for a trait. So the homozygous recessive individual can pass on only recessive alleles to an offspring. The heterozygous individual has one dominant and one recessive allele for the gene for a trait. So the heterozygous individual can pass on either a dominant or a recessive allele to an offspring. So if an offspring inherits a recessive allele from the heterozygous parent, along with the recessive allele from the homozygous recessive parent, it will have the homozygous recessive genotype and phenotype.
A harmful recessive allele remains in the population because both homozygous dominant and heterozygous genotypes produce the dominant, healthy phenotype. So the heterozygous genotype keeps the harmful recessive allele in the population.
He would have the recessive phenotype for that trait.
because it dominates the phenotype
A genotype in which there are both a dominant and a recessive allele is called heterozygous.
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.
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.