You can be a carrier of a recessive gene as part of your genotype.
She is a carrier of hemophilia but does not have the condition
If their genotype contains both a dominant and a recessive allele for a trait.
Their genotype would be Tt for Tay-Sachs, with one copy of the normal gene (T) and one copy of the mutated gene (t).
The genotype of a person with CF is cc. The genotype of a carrier of a CF mutation is Cc.
The genotype of a person who is a carrier of an autosomal recessive trait is typically heterozygous, meaning they carry one copy of the recessive allele and one copy of the dominant allele for that trait. This would be represented as Aa, with the lowercase "a" representing the recessive allele.
If an AC genotype man and an AS genotype woman marry, each of their children has a 25% chance of being born with a sickle cell disease (SS genotype), a 50% chance of being a carrier like their parents (AS genotype), and a 25% chance of having a normal genotype (AA).
I think no. It's caused by a recessive gene so if a person has albinism their genotype can only be recessive, recessive ---> AA (small a small a or whatever you call it). No other genotype will mean that person has Albinism, like if it has at least one big A, that means it's just a carrier of albinism.
A genotype that is heterozygous means an individual has two different alleles for a particular gene. This can result in a mix of traits or characteristics, earning the term "hybrid" from the blending of genetic information. In cases where one allele is dominant and the other recessive, the individual may not exhibit the recessive trait but can pass it on to offspring, hence being referred to as a "carrier."
Mary's father is normal and has a normal genotype XY while her mother is the carrier of hemophilia and has one X of her genotype infected i.e. she is X*X.
She is a carrier of hemophilia but does not have the condition
I think it's genotype...