N-normal
l-lethal
Nl
so, dominant normal and recessive lethal, making him/her normal but carries a lethal allele.
In sex-linked traits, slashes are used to designate the sex of an individual and the genotype for a specific trait. For example, in females with two X chromosomes and a recessive allele for a trait, the genotype would be represented as X^bX^b (affected) or X^BX^b (carrier). In males, the genotype is represented with just one X chromosome, as in X^bY (affected) or X^BY (unaffected).
if someone is a Heterozygous carrier of Tay-Sachs they would have to be Tt. Because TT is Homozygous.
You cannot do a cross to determine the genotypes of individuals because there is only one gene here. Genotype consists of the entire genetic makeup of the individual, which cannot be determined by a single gene. Only the alleles S or s is used to express this particular gene. If you're looking for a monohybrid cross between Ss and Ss, while separately wanting a result between ss and ss, then the answers are as follows: Ss x Ss 25% SS 50% Ss 25% ss ss x ss = 100% ss
The blood test is called a hemoglobin electrophoresis test, which is used to determine an individual's hemoglobin genotype. A result of 'AA' indicates normal hemoglobin, 'AS' indicates sickle cell trait (carrier), and 'SS' indicates sickle cell disease.
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.
The carrier typically remains unaffected by the disorder.
Rr heterozygous
You can be a carrier of a recessive gene as part of your genotype.
In sex-linked traits, slashes are used to designate the sex of an individual and the genotype for a specific trait. For example, in females with two X chromosomes and a recessive allele for a trait, the genotype would be represented as X^bX^b (affected) or X^BX^b (carrier). In males, the genotype is represented with just one X chromosome, as in X^bY (affected) or X^BY (unaffected).
She is a carrier of hemophilia but does not have the condition
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."
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 Punnett square for cystic fibrosis would involve crossing two parents who are carriers of the recessive allele for the disease (denoted as "cf"). The square would show the probability of having a child with cystic fibrosis (25%), a carrier (50%), or unaffected by the disease (25%). Each parent would have a genotype of "Cf" (carrier) for the Punnett square.
If their genotype contains both a dominant and a recessive allele for a trait.
A carrier. This individual may not show the undesirable trait, but can pass on the recessive allele to their offspring.
What is a heterzygous individual?
if someone is a Heterozygous carrier of Tay-Sachs they would have to be Tt. Because TT is Homozygous.