The gene codes for a protein called huntingtin found on the short arm of chromosome 4.
# 4
Yes, #4.
An allele is an alternative form of a gene that is found at the same location on a chromosome.
No. Hemophilia is the result of any of a number of mutations such as reversals, translations, deletions, etc. These mutations need to have occurred in a very specific segment of the coding found on the X chromosome. The replication of that X chromosome however is unaffected with the exception that the mutation on it is replicated as well.
The unit of heredity found on a chromosome is called a gene.
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.
A gene found on a sex chromosome is known as a sex-linked gene. Alleles are the different forms of a gene.
It isn't - it's found on one of your autosomes: the 22 non-sex chromosomes. It's found on the fourth chromosome.
The hunt for the gene was accomplished by the work of many dedicated researchers working cooperatively.
Hemophilia is a recessive allele condition. Men can get hemophilia alot easier than women as the allele is found on the XY Chomosome pair. With men. they do not have the extra "tail" on the Y chromosome compared to the XX with a female. If the person has the recessive allele on the X chromosome and this person is male, they will be a hemophiliac as they do not have a 'pair' allele which could be dominant to stop the condition expressing itself. On a female, if there is a recessive (hemophilia) allele on one of the X chromosomes but on the other is a Dominant (normal) allele then she will be a carrier of the faulty gene but will not suffer from the condition herself. If the female have a recessive (faulty) gene on each of the XX chromosomes, then she will be a sufferer of the disease.
It is a mutated gene called PKD1 located on chromosome 16.
Males, because they have one X chromosome, in which the traits are carried on. Therefore, if they have one allele they will have that trait because they do cannot have another allele to affect it.
Chromosome numbers: 1, 14, 19, and 21 are affected by Alzheimer's disease.
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