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What else can I help you with?
Is a person who is homozygous recessive for a recessive genetic disese a carrier?
As long as a persons genotype consists of at least one recessive gene, they can pass it on to offspring to give them the disease, which makes them a carrier. Since this persons genes are both recessive, it is definite that they will pass on the recessive gene.
What type of alleles does a person considered a Carrier have?
A person considered a carrier typically has one normal (dominant) allele and one mutated (recessive) allele for a specific gene. This means they do not exhibit symptoms of the genetic condition associated with the recessive allele but can pass the mutated allele to their offspring. For example, in autosomal recessive disorders, carriers are asymptomatic but can potentially have affected children if their partner is also a carrier.
What genotype must the person have who possessed the recessive phenotypes?
The genotype is homozygous recessive or the recessive trait is on the X chromosome and has no corresponding allele on the Y chromosome.
A scientist notices that a person has two recessive genes for a trait This describes the person's?
genotype for that trait.
Is it true that if a person has a recessive trait the genotype must be homozygous recessive for the trait?
Yes, if a person expresses a recessive trait, their genotype must be homozygous recessive for that trait. This means that they have two copies of the recessive allele, one from each parent. If they were heterozygous they would not display the trait.
What is the genotype of an individual with albinism?
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.
Is a person who is homozygous recessive for a recessive genetic disese a carrier?
As long as a persons genotype consists of at least one recessive gene, they can pass it on to offspring to give them the disease, which makes them a carrier. Since this persons genes are both recessive, it is definite that they will pass on the recessive gene.
What type of alleles does a person considered a Carrier have?
A person considered a carrier typically has one normal (dominant) allele and one mutated (recessive) allele for a specific gene. This means they do not exhibit symptoms of the genetic condition associated with the recessive allele but can pass the mutated allele to their offspring. For example, in autosomal recessive disorders, carriers are asymptomatic but can potentially have affected children if their partner is also a carrier.
What would be the genotype of a person with cystic fibrosis?
The genotype of a person with CF is cc. The genotype of a carrier of a CF mutation is Cc.
What genotype must the person have who possessed the recessive phenotypes?
The genotype is homozygous recessive or the recessive trait is on the X chromosome and has no corresponding allele on the Y chromosome.
A scientist notices that a person has two recessive genes for a trait This describes the person's?
genotype for that trait.
Is sickle cell anemia an autoimmune disease?
Sickle Cell Anemia is Autosomal Recessive. It arises from a mutation on the beta-globin gene of chromosome 11. Because Sickle Cell Anemia is an example of incomplete dominance, a person has the disease if they have two mutated beta-globin genes but only has the trait (is a carrier) if they have only one mutated beta-globin gene.
Is it true that if a person has a recessive trait the genotype must be homozygous recessive for the trait?
Yes, if a person expresses a recessive trait, their genotype must be homozygous recessive for that trait. This means that they have two copies of the recessive allele, one from each parent. If they were heterozygous they would not display the trait.
A person who has inherited the autosomal recessive disorder called?
A person who has inherited an autosomal recessive disorder will have two copies of the mutated gene, one from each parent. This results in the individual expressing the disorder. Symptoms can vary depending on the specific disorder.
How are Genotype phenotype different?
Phenotypes are the traits expressed by the genotype. So, for blood type, a person can have A and i alleles (genotype). However, in the phenotype, since i is recessive, only the A will be expressed, and the person will have an A blood type.
An example of a heterozygous recessive genotype is?
An example of a heterozygous recessive genotype is when an individual carries one dominant allele and one recessive allele for a particular trait. One example could be a person with the genotype Aa, where "A" represents the dominant allele and "a" represents the recessive allele.
Who is a person that is a carrier for a sex-linked recessive disorder?
Usually female.
