When taking two alles as A and a. They are AA and Aa
The phenotype would be the dominant trait.
Tt or TT
Two diffrent alleles at a locus, are responsible for diffrent phenotypes and both affects the phenotype
Phenotypes are the entirety of the observable traits. Genotypes are the instructions in the genetic code. Dominant alleles override the recessive alleles, making only the dominant alleles expressed.
Aa AA aa If A dominant, two phenotypes.
Capital letters usually denote dominant alleles. Therefore QQ genotype would contain two dominant alleles for the Q genotype.
Homozygous Dominant or Homozygous Recessive, accordingly.
Two diffrent alleles at a locus, are responsible for diffrent phenotypes and both affects the phenotype
The genotypes in which one or more alleles is dominant.
Phenotypes are the entirety of the observable traits. Genotypes are the instructions in the genetic code. Dominant alleles override the recessive alleles, making only the dominant alleles expressed.
Aa AA aa If A dominant, two phenotypes.
wha- dominant? alleles?
This would depend upon how they are expressed. Are we talking dominant, codominant, or recessive? Then there are genes thought to be fine tuned by environmental factors.
In eyes, it would be brown is dominant, and blue is recessive. Free earlobe allele is said to be dominant over the attached earlobe allele. When an organism has two dominant alleles for a trait, it is called homozygous dominant. Two recessive alleles for a trait is homozygous recessive.
Capital letters usually denote dominant alleles. Therefore QQ genotype would contain two dominant alleles for the Q genotype.
A gene pair that consists of 2 dominant or 2 recessive alleles is considered homozygous dominant or homozygous recessive.
Homozygous Dominant or Homozygous Recessive, accordingly.
phenotypes are decided by the alleles for that particular characteristic, by a dominant or two recessive alleles. For example, cystic fibrosis has a recessive allele so the phenotype of cystic fibrosis would only appear if there were two of the recessive allele, one from each parent, were present. A heterozygous carrier of the cystic fibrosis allele would show the phenotype of not having cystic fibrosis. So to determine the phenotype simply find out which allele is dominant and find what alleles each parent has the the probability of each phenotype can be calculated
Co-dominant allele is the one that shows dominance with another allele from a different loci. Basically its one of the following: 1) two different alleles at a locus are responsible for different phenotypes. 2) two alleles that affect the phenotype of the heterozygote. For instance ab blood groups