chromosome 17 The correct answer is chromosome 15
No, Parkinson's disease is not caused by a mutation on chromosome 6. The exact cause of Parkinson's disease is not fully understood, but it is believed to involve a combination of genetic and environmental factors. Some rare forms of Parkinson's disease are linked to specific gene mutations, but these are not located on chromosome 6.
There are multiple genes encoded by this chromosome. The duplication of the chromosome might have dysregulated multiple genes that affect the patterning of the head and body and affect wing pigmentation. On the other hand, one gene might be involved in all these processes. For instance, patients with Down syndrome have three copies of chromosome 21, resulting in developmental issues but also an early onset of Alzheimers Disease.
The allele that is responsible of Fabry Disorder/Disease is located on the X chromosome and is the only lipid storage disorder identified as being sex linked.
The X chromosome contains considerably more genetic material than the Y chromosome.
An individual with a recessive disease-causing allele on one chromosome and a normal allele on the other chromosome is referred to as a heterozygote for that gene. Since the disease is recessive, the normal allele typically masks the effects of the recessive allele, meaning the individual usually does not exhibit symptoms of the disease. However, they can still pass the recessive allele to their offspring.
recessive
14q31
2-21
Tay-Sachs disease is caused by a genetic mutation in the HEXA gene on (human) chromosome 15 and no other chromosome is involved.
Chromosome 4
Gaucher's disease is located on chromosome 1, which is not the sex chromosome, so no. It is not a sex linked disease.
Arthritis does not effect a chromosome.
No, Parkinson's disease is not caused by a mutation on chromosome 6. The exact cause of Parkinson's disease is not fully understood, but it is believed to involve a combination of genetic and environmental factors. Some rare forms of Parkinson's disease are linked to specific gene mutations, but these are not located on chromosome 6.
It's Chromosome X .
Chromosome 16 has been a target of study by Crohns disease researchers lately and Chromosome 16 probably contains between 850 and 1,200 genes.
Chromosome numbers: 1, 14, 19, and 21 are affected by Alzheimer's disease.
There are multiple genes encoded by this chromosome. The duplication of the chromosome might have dysregulated multiple genes that affect the patterning of the head and body and affect wing pigmentation. On the other hand, one gene might be involved in all these processes. For instance, patients with Down syndrome have three copies of chromosome 21, resulting in developmental issues but also an early onset of Alzheimers Disease.