The phenotype associated with a recessive gene is only expressed when two copies of the gene are present. For example, if a person has both a recessive allele and a dominant allele for CF, the person does not have CF. The person only has CF if he/she has two copies of the recessive allele.
CF is recessive, and as such, the gene for non-CF is dominant over this gene. The CF gene will only be expressed in the phenotype and as a characteristic if the person has two of the recessive alleles.
Cystic fibrosis (CF) is an autosomal recessive disorder, not an X-linked disorder. It means that both copies of the gene responsible for CF need to be mutated in order to develop the disorder. Incomplete dominance refers to a genetic trait where the heterozygous condition results in an intermediate phenotype, which is not the case for CF.
Let's do a Punnit Square. T T T TT TT t Tt Tt T is normal, and the little "t" is the recessive gene (which is being carried by one parent). Since one parent is recessive, you can see that there's a 50% chance that the offspring will have the recessive gene as well. However, note that without any straight "tt" result, there is a 0% chance that the offspring can express the Tay Sachs disorder.
If the recessive gene is present in both of the parents.
Most genes have two copies of each gene with dominant gene "trumping" the recessive one. The gene is recessive because it is said not to do much of anything unless paired with another recessive gene, but if paired with a dominant gene, the dominant gene wins.
Cystic Fibrosis is recessive. If you have one CF gene and one non-CF gene, you will be a carrier but not have CF.
CF is recessive, and as such, the gene for non-CF is dominant over this gene. The CF gene will only be expressed in the phenotype and as a characteristic if the person has two of the recessive alleles.
Cystic fibrosis (CF) is an autosomal recessive disorder, not an X-linked disorder. It means that both copies of the gene responsible for CF need to be mutated in order to develop the disorder. Incomplete dominance refers to a genetic trait where the heterozygous condition results in an intermediate phenotype, which is not the case for CF.
Let's do a Punnit Square. T T T TT TT t Tt Tt T is normal, and the little "t" is the recessive gene (which is being carried by one parent). Since one parent is recessive, you can see that there's a 50% chance that the offspring will have the recessive gene as well. However, note that without any straight "tt" result, there is a 0% chance that the offspring can express the Tay Sachs disorder.
The genotype of a person with CF is cc. The genotype of a carrier of a CF mutation is Cc.
if u have a recessive gene with a recessive gene then u can see the recessive gene but if you have a dominant gene with a recessive gene you can only see the dominant gene hope that helps:)
If the recessive gene is present in both of the parents.
Most genes have two copies of each gene with dominant gene "trumping" the recessive one. The gene is recessive because it is said not to do much of anything unless paired with another recessive gene, but if paired with a dominant gene, the dominant gene wins.
Recessive, as in recessive genes, refers to an inherited characteristic or trait that is expressed only when two copies of the gene responsible for it are present.
recessive.
You don't have it but have the gene and are a carrier and could pass it on.
The parents will both have a specific gene defect. If they do there is then a 1 in 4 chance of them having a child with cf. so if you are considering having children you should have a blood test to find out if you are a carrier of the gene causing cf. hope that helps.