If you are looking to see what happens to a specific trait, this is not actually an answerable question in this context. It is so open-ended. Also, parents are not directly homozygous or heterozygous, the genes are. However, in the simplest case, half of the offspring would be homozygous for the gene in question and half would be heterozygous. How this affects the phenotypic trait under observation depends on a lot of other things.
Allele frequency is stable.(Apex)
An allele is an alternative form of a gene that is found at the same location on a chromosome.
if the two alleles are the same in the same box in the punnett square then that trait is expressed. when there is a double in a punnett square then that gene is always expressed
When two mutants with the same phenotype are crossed and the progeny exhibit a wild-type phenotype, it suggests that the mutations are likely in the same gene and are recessive. This means that both parental mutants are homozygous for the same recessive allele, and when combined, they produce offspring with the dominant wild-type phenotype. Therefore, the mutations are allelic to each other.
Homozygous individuals have two identical alleles for a particular gene, while heterozygous individuals have two different alleles for the same gene. Homozygotes can be either homozygous dominant (two dominant alleles) or homozygous recessive (two recessive alleles), while heterozygotes have one dominant and one recessive allele.
One way is if an allele for the gene in question is dominant. Homozygotes for the dominant allele and heterozygotes will both have the same phenotype.Organisms have the same phenotype, or physical characteristics. They do not, however, have the same genotype, or genetic makeup. If T represent tall, and t represnts short then the organism will have the genotypes TT and Tt. If you make a Punnett square you will have the same phenotype but different genotypes. Unless some weird mutation occurs....
Allele frequency is stable.(Apex)
The bases in one allele is different from bases in another allele because an allele is different forms of the same gene. This means that even though they have been programed for the same thing there is a variation
An allele is an alternative form of a gene that is found at the same location on a chromosome.
if the two alleles are the same in the same box in the punnett square then that trait is expressed. when there is a double in a punnett square then that gene is always expressed
The individual with two of the same allele is "homozygous" for a trait.
Do you mean allele? An allele is a different molecular form of the same gene.
When two mutants with the same phenotype are crossed and the progeny exhibit a wild-type phenotype, it suggests that the mutations are likely in the same gene and are recessive. This means that both parental mutants are homozygous for the same recessive allele, and when combined, they produce offspring with the dominant wild-type phenotype. Therefore, the mutations are allelic to each other.
Homozygous individuals have two identical alleles for a particular gene, while heterozygous individuals have two different alleles for the same gene. Homozygotes can be either homozygous dominant (two dominant alleles) or homozygous recessive (two recessive alleles), while heterozygotes have one dominant and one recessive allele.
When Mendel crossed a true-breeding short plant with a true-breeding tall plant, all the offspring were tall. Which term describes the gene for tallness?
A dominant allele located on an autosome will be expressed phenotypically in the individual, meaning it will be visible in the physical characteristics of the organism. This dominant allele will mask the effects of any recessive allele at the same locus.
an allele