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What chromosome is nail patella syndrome found on?
Nail Patella Syndrome is found on chromosome #9. If you search "what chromosome is nail patella syndrome on?" in Google, then it will give you a bunch of websites that have a bunch of info. about it. hope this helps. :-)
In all conditions where a defective gene is on the X chromosome transmission to a female can be through the mother or Father?
In cases where a defective gene is located on the X chromosome, a female can inherit the gene from either parent. If the mother carries one defective X chromosome, she can pass it on to her daughter. Similarly, if the father has the defective gene on his single X chromosome, he will pass it to all his daughters, as they inherit his X chromosome. Therefore, females can receive the defective gene from both maternal and paternal sources.
On what chromosome is tourette syndrome located on?
They don't know yet, Recent research suggests that a small number of Tourette syndrome cases may be caused by a defect on chromosome 13 of gene SLITRK1. and some other chromosomes like 7. There now busy with a study to find the genes that may cause tourette syndrome, results will be given by 2018
What chromosomes are affected with hurler syndrome?
Hurler syndrome is caused by a mutation in the gene located on chromosome 4 that provides instructions for producing an enzyme called alpha-L-iduronidase. This mutation leads to the accumulation of glycosaminoglycans in the body, resulting in the various symptoms associated with the syndrome.
What chromosome is Proteus syndrome located?
Proteus syndrome is not caused by a specific gene on a particular chromosome; instead, it is thought to be due to a somatic mutation (mutation occurring after fertilization) in the AKT1 gene. This mutation leads to overgrowth of certain tissues in the body, resulting in the characteristic features of the syndrome.
What chromosome is Wiskott-Aldrich syndrome on?
It's located on the X chromosome.
What chromosome is nail patella syndrome found on?
Nail Patella Syndrome is found on chromosome #9. If you search "what chromosome is nail patella syndrome on?" in Google, then it will give you a bunch of websites that have a bunch of info. about it. hope this helps. :-)
What chromosome is klinefelters syndrome located on?
they have a extra chromosome, a normal male is XY, a male with klinefelters is XXY.
In all conditions where a defective gene is on the X chromosome transmission to a female can be through the mother or Father?
In cases where a defective gene is located on the X chromosome, a female can inherit the gene from either parent. If the mother carries one defective X chromosome, she can pass it on to her daughter. Similarly, if the father has the defective gene on his single X chromosome, he will pass it to all his daughters, as they inherit his X chromosome. Therefore, females can receive the defective gene from both maternal and paternal sources.
On what chromosome is tourette syndrome located on?
They don't know yet, Recent research suggests that a small number of Tourette syndrome cases may be caused by a defect on chromosome 13 of gene SLITRK1. and some other chromosomes like 7. There now busy with a study to find the genes that may cause tourette syndrome, results will be given by 2018
What chromosome is gene located for marfan syndrome?
The gene associated with Marfan syndrome is located on chromosome 15. It is called the FBN1 gene, which provides instructions for making a protein called fibrillin-1. Mutations in this gene can lead to the characteristic features of Marfan syndrome.
Dose marfan syndrome have to be on a x chormose?
Marfan syndrome is caused by a mutation in the FBN1 gene, which is located on chromosome 15 and is inherited in an autosomal dominant pattern. It is not linked to the X chromosome. Both males and females can inherit and display symptoms of Marfan syndrome.
Why does Lesch-Nyhan syndrome affect males?
Lesch-Nyhan syndrome is an X-linked recessive disorder, meaning the gene mutation responsible for the condition is located on the X chromosome. Males have one X chromosome and one Y chromosome, so if they inherit the mutated gene on their X chromosome, they will develop the disorder. Females have two X chromosomes, so they are less likely to inherit the mutation on both X chromosomes.
What chromosomes are affected with hurler syndrome?
Hurler syndrome is caused by a mutation in the gene located on chromosome 4 that provides instructions for producing an enzyme called alpha-L-iduronidase. This mutation leads to the accumulation of glycosaminoglycans in the body, resulting in the various symptoms associated with the syndrome.
Is marfan syndrome carried on the x or y chromosome or both?
Marfan syndrome is typically inherited in an autosomal dominant pattern, meaning that a mutation in a single copy of the gene is enough to cause the disorder. It is not specifically located on the X or Y chromosome.
What chromosome is Proteus syndrome located?
Proteus syndrome is not caused by a specific gene on a particular chromosome; instead, it is thought to be due to a somatic mutation (mutation occurring after fertilization) in the AKT1 gene. This mutation leads to overgrowth of certain tissues in the body, resulting in the characteristic features of the syndrome.
What gene is affected by Barth syndrome?
Barth syndrome occurs when a person is born with a mutated, or abnormal, TAZ1 (or G4.5) gene. This abnormal gene is located on the X chromosome, which is a sex-determining chromosome. Males have one X and one Y chromosome, while females have two X chromosomes.
