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Yosef's Genes
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∙ 10y ago
Raquel Cukierkorn
SLITRK1
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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.
What is xp21 gene?
Dystrophin gene / Xp21 gene / DMD gene: Found at locus Xp21 of the X chromosome, this is why it's called the (Xp21 gene) It's the gene responsible for Duchenne muscular dystrophy(DMD) when mutated, this is why it's called (DMD gene)
What is the sry gene?
The SRY gene is a gene on the Y chromosome required for the development of testes. It stands for Sex determining Region on Y chromosome.
Whats a change in gene or chromosome?
A change in a gene or chromosome is called a: Mutation
What does it mean to say that a gene is linked to a chromosome?
This means that the gene is physically located on that particular chromosome.
What chromosome is polycystic kidney disease found?
It is a mutated gene called PKD1 located on chromosome 16.
What gene or chromosome is mutated in the hemophilia disorder?
There are two types of hemophilia. Type A: A mutation in the factor VIII gene. Type B: A mutation in the IX gene.
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.
What chromosome number is affected in Lowe syndrome?
Lowe syndrome is caused by a mutated gene on the X sex chromosome. Because it is X-linked, it occurs almost exclusively in males.
What is xp21 gene?
Dystrophin gene / Xp21 gene / DMD gene: Found at locus Xp21 of the X chromosome, this is why it's called the (Xp21 gene) It's the gene responsible for Duchenne muscular dystrophy(DMD) when mutated, this is why it's called (DMD gene)
Is fragile x syndrome sex linked?
Yes. It is found as a mutation on the X chromosome (a sex chromosome) so it is sex linked. The gene for Fragile X is carried on the X chromosome. Because both males (XY) and females (XX) have at least one X chromosome, both can pass on the mutated gene to their children.
What various types of genetic material in order from simplest to most complex?
nucleus → chromosome → gene
List these in order from smallest to largest chromosome gene cell?
Smallest to largest: Gene (a place on a chromosome); chromosome (there are 46 in human cells); and DNA (because it accounts for all the genetic material in a cell).
What is a changed gene?
mutated
Does Fibrodysplasia Ossificans Progressiva have a bad chromosome?
The gene that is mutated in a person who has Fibrodysplasia Ossificans Progressiva is called the ACVR1 gene. A small mutation in one of the two copies of the ACVR1 gene modifies the meaning of its genetic message, so a defective protein is made.
What most mutated genes are which cause human disorders?
A mutated gene is just a gene that doesn't have the correct DNA or alleles.. Depending of the human disorder the gene that is mutated will be different... We use genes throughout our bodies but ALL genes can cause human disorders but there is NO single gene that, when mutated, creates ALL genetic modification...
Gene is it the same as a chromosome?
no, the gene is not actually the chromosome but a part of chormosome...
