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Sickle cell disease is an autosomal reccessive sexlinked trait so, a female msut have 2 recessive alleles to have the trait and a male needs only one allele (this is because there is no corresponding site for this allele on the Y chromosome.
The female can be a carrier of the disorder with the defective allele on one X chromosome and a normal allele on the other X chromosome. Female carrriers can have a mixture of normal and abnormal redblood cells.
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What is the multiple allele system?
The multiple allele system refers to a genetic system where a particular gene has more than two alleles present within a population. Each individual carries a maximum of two alleles for a gene, but the population as a whole may have multiple alleles. An example of this is the ABO blood group system in humans.
What is the difference between a gene allele Chromosome and trait?
Alleles are alternate versions of genes that code for certain phenotypes, or traits. The traits of an individual are a result of the interaction between their genotype (alleles) and the environment.
Hurlington disease is an autosomal dominant disorder that affects the nervous system if a man is heterozygous for the alleles that cause the condition and has children with a woman who lacks then?
If a man who is heterozygous for the Hurlington disease alleles has children with a woman who does not have the alleles, there is a 50% chance that each of their children will inherit the disease allele. Since Hurlington disease is autosomal dominant, inheriting just one copy of the disease allele will result in the individual being affected by the disorder.
How come there are no carriers in genetic diseases caused by dominant alleles?
If carried on a dominant allele, you either inherit it- and have the disease- or you don't- and do not have the disease, nor the gene that causes it. If you don't have the gene, you can not pass it to your offspring.
If a man is heterozygous for the alleles that cause the condition and has children with a woman who lacks that defective allele?
If a man is heterozygous for the alleles that cause the condition and has children with a woman who lacks that defective allele, there is a 50% chance that each of their children will inherit the defective allele. This is because the man can pass on either the normal or defective allele, resulting in a 50% chance of passing on the defective allele.
Is huntington's disease determined by multiple alleles?
No. This is a single gene disorder. If at least one allele has the huntington's mutation, the person will eventually develop the disease.
What is contributing allele?
A contributing allele is a genetic variant that is associated with a particular trait or disease. These alleles can have a small to moderate effect on the trait, increasing or decreasing the likelihood of developing that trait. Multiple contributing alleles can interact to determine the overall phenotype of an individual.
What is the multiple allele system?
The multiple allele system refers to a genetic system where a particular gene has more than two alleles present within a population. Each individual carries a maximum of two alleles for a gene, but the population as a whole may have multiple alleles. An example of this is the ABO blood group system in humans.
What is an example of multiple allele heredity?
An allele is a type of gene that is hereditory. In fertilisation, an allele from both the father and mother are fused, this is multiple allele hereditory. Alleles influence many things, from hair colour to blood type. human blood typeshuman blood types
What is the difference between a gene allele Chromosome and trait?
Alleles are alternate versions of genes that code for certain phenotypes, or traits. The traits of an individual are a result of the interaction between their genotype (alleles) and the environment.
What are some examples of allele's?
Multiple alleles means that for a specific locus on a chromosome there can be 3 or more forms of that gene (allele). Only one allele can be inherited because they are found on homologous chromosomes. Height is not a multiple allele because it is associated with many genes on several chromosomes (plus environmental factors) so this would be polygenic inheritance. Multiple allele trait is the ABO group. The allele for A B or O (3 alleles ) is found on the same locus, therefore only one of them could be inherited EXAMPLE: DNA
Hurlington disease is an autosomal dominant disorder that affects the nervous system if a man is heterozygous for the alleles that cause the condition and has children with a woman who lacks then?
If a man who is heterozygous for the Hurlington disease alleles has children with a woman who does not have the alleles, there is a 50% chance that each of their children will inherit the disease allele. Since Hurlington disease is autosomal dominant, inheriting just one copy of the disease allele will result in the individual being affected by the disorder.
When than two alleles control a trait?
The presence of more than two alleles that control a trait is called multiple allele. An example of this is the group gene of ABO blood that has three alleles.
What is an example of multiple alleles?
An example of multiple alleles is the ABO blood system in humans, where the gene for blood type has three alleles: A, B, and O. Each person inherits two of these alleles, resulting in four possible blood types: A, B, AB, and O.
When more than two different alleles control a trait?
This phenomenon is known as multiple allelism, where there are more than two different variations of a gene (alleles) that can affect a single trait. In this case, individuals can inherit one of several possible alleles for the trait. Examples include the ABO blood group system in humans, where there are three alleles (IA, IB, i) that determine a person's blood type.
What is meaning of alleles?
An allele is the different forms of a gene. For example the gene for eye colour has the alleles; brown, blue, green etc. In every person there are two alleles for every gene but both alleles are not always the same. They can be dominant and recessive; dominant alleles are expressed no matter what other allele is present, recessive alleles require both alleles to be the recessive one to be expressed. E.g. say B is the allele for brown eyes and b is the allele for blue eyes. Brown is dominant therefore if someone had Bb or BB they'd have brown eyes and if they had bb their eyes would be blue.
How come there are no carriers in genetic diseases caused by dominant alleles?
If carried on a dominant allele, you either inherit it- and have the disease- or you don't- and do not have the disease, nor the gene that causes it. If you don't have the gene, you can not pass it to your offspring.
