Women have two X chromosomes, while men have an XY chromosome, therefore if the recessive allele is on the X chromosome, the man will most likely inherit the gene. While the woman has two X's, I believe because it is recessive both X's have to contain the allele. So if only one X has a recessive allele, she will not inherit it.
Huntingdons chorea is caused by a dominant allele.
Autosomal dominant allele
The traits inherited depends upon the alleles that have been passed on from the father and mother.The traits that are exhibited is called as the phenotype. Dominant allele needs only one copy to be expressed.For example in a pea plant "T" represents the tall dominant allele and "t" the short recessive allele .TT - when there are two dominant alleles the pea plant will express the tall trait. The pea plant is tall.Tt - when there is one dominant and one recessive allele the pea plant will still express the tall trait.In this case the dominant allele masks the recessive allele and the pea plant is still tall.tt - when there are two recessive alleles the pea plant will express the recessive trait and the pea plant is short.For a recessive trait to show up there should be a pair of recessive alleles.
a example of a gene
Genetic Disorders are caused By a change in a person's DNA. Recessive alleles is the most human genetic disorder.
well some people believe a birthmark is caused by a recessive allele on the y chromosome
Huntingdons chorea is caused by a dominant allele.
No. It is caused by a recessive allele on the X chromosome.
If 4% of males in a population have red-green color blindness, then the allelic frequency is 4% in males and in females. If mating is random, then in females, 92.16% do not carry the allele on either X chromosome, 7.68% carry the allele on one X chromosome, and 0.16% carry the allele on both X chromosomes. We have the dominant allele with frequency p and the recessive allele with frequency q, so 0.9216 + 0.0768 + 0.0016 = p^2 + 2pq + q^2 = (p + q)^2 = (0.96 + 0.04)^2
An individual (male) with an allele on the X chromosome but no corresponding allele on the Y chromosome is described as hemizygous. Genes which are inherited in this way are described as sex-linked or X-linked. An example is hemophilia - the inability of the blood to clot. It is caused by a recessive allele, so males only need to inherit one copy to develop the characteristic. Females can inherit one hemophilia allele and one normal allele, so they can act as carriers of the disease without developing it themselves. See http://en.wikipedia.org/wiki/X-linked_gene
yes
Autosomal dominant allele
It is caused by a recessive allele. Believe me my teacher told me.
this disease is caused by a recessive allele that is found only on the x chromosome. a human female has two x chromosomes. a human male only has 1 x chromosome. therefore, a male needs only one recessives allele to have hemophilia, while a female needs two recessive allele. as a result, hemophilia is much more common in males.
This disease results from a mutation on the x-chromosome. It's recessive considering that a dominant will only cover up things that have occur, for example the damage that has occured, with something else. A recessive will continue to give latent traits. The allele in Adrenoleukodystrophy can only be caused by heredity mutation thus making it recessive.
Huntington's disease is caused by a dominant allele
The same number as any other human as the condition is not caused by the absence of an entire chromosome. 90% of cases are caused by an autosomal recessive of the CYP21 allele. So far there are at least 56 identified variations at this site that can cause the many variations of CAH.