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The genotype Rr represents an individual that carries one dominant allele (R) and one recessive allele (r) for a specific trait. This individual is called heterozygous for that trait.
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.
The genotype for an individual who is heterozygous for both traits of tongue rolling and cleft chin would be RrCc. "R" represents the dominant allele for tongue rolling and "r" represents the recessive allele for non-tongue rolling, while "C" represents the dominant allele for cleft chin and "c" represents the recessive allele for no cleft chin.
A heterozygous genotype for a dihybrid is when an individual has different alleles for both traits being considered. For example, in the case of eye color (trait 1) and hair color (trait 2), a heterozygous genotype might be EeBb, where "E" represents one allele for eye color and "e" represents another, while "B" represents one allele for hair color and "b" represents another.
"Tt" typically represents a heterozygous genotype with one dominant allele (T) and one recessive allele (t). In this case, the dominant allele would determine the dominant phenotype.
A heterozygous allele combination is typically shown using letters to represent the alleles of a gene. For example, if the alleles for a gene are "A" and "a," a heterozygous individual would be represented as "Aa." This signifies that the individual has one copy of each allele.
The genotype Rr represents an individual that carries one dominant allele (R) and one recessive allele (r) for a specific trait. This individual is called heterozygous for that trait.
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.
The genotype for an individual who is heterozygous for both traits of tongue rolling and cleft chin would be RrCc. "R" represents the dominant allele for tongue rolling and "r" represents the recessive allele for non-tongue rolling, while "C" represents the dominant allele for cleft chin and "c" represents the recessive allele for no cleft chin.
An example of a heterozygous recessive genotype is when an individual carries one dominant allele and one recessive allele for a particular trait. One example could be a person with the genotype Aa, where "A" represents the dominant allele and "a" represents the recessive allele.
A heterozygous genotype for a dihybrid is when an individual has different alleles for both traits being considered. For example, in the case of eye color (trait 1) and hair color (trait 2), a heterozygous genotype might be EeBb, where "E" represents one allele for eye color and "e" represents another, while "B" represents one allele for hair color and "b" represents another.
The notation Tt represents a heterozygous genotype for the trait of being tall, where T is the dominant allele for tallness and t is the recessive allele for shortness. This means the individual will exhibit the tall trait because the dominant allele is 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.
In a heterozygous IAi person, the IA allele is dominant over the i allele. This means that the phenotype will show the IA allele's trait as it masks the expression of the recessive i allele.
Having one allele for tall stems and one allele for short stems is a heterozygous genotype and could be represented as Tt, where T represents the tall allele, and t represents the short allele, if the tall allele has complete dominance over the short allele.
A genotype in which there are both a dominant and a recessive allele is called heterozygous.
An allele that produces a heterozygous condition is one where an individual carries two different versions of a gene at the same locus. This can result in a combination of traits from both alleles, often leading to a phenotype that is a mix of the two versions.