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It is caused by a gene mutation in the single gene on chromosome 7 that produces a protein known as CFTR.

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What kind of pathogen causes Cystic Fibrosis?

Cystic Fibrosis is caused by a genetic mutation in the CFTR gene. This mutation leads to the production of thick, sticky mucus in the lungs and other organs. It is not caused by a specific pathogen, but individuals with Cystic Fibrosis are more susceptible to respiratory infections.


True False Cystic fibrosis is caused by a mutation that is the dominant allele of a gene?

False. Cystic fibrosis is caused by a mutation in the CFTR gene, which is a recessive allele. An individual must inherit two copies of the mutated gene (one from each parent) to develop the condition.


What is the sequence of amino acid in cystic fibrosis?

The sequence of amino acids in cystic fibrosis is caused by a mutation in the CFTR gene, which leads to the production of a faulty cystic fibrosis transmembrane conductance regulator protein. This mutated protein results in abnormal function, leading to the characteristic symptoms of cystic fibrosis such as thick mucus production.


Does cystic fibrosis have extra chromosomes?

No, cystic fibrosis is caused by mutations in the CFTR gene, not by the presence of extra chromosomes. Individuals with cystic fibrosis inherit two faulty copies of the CFTR gene, one from each parent, which leads to the production of a defective CFTR protein that affects the movement of salt and water in and out of cells.


What does CFTR-ΔF508 refer to?

CFTR-ΔF508 refers to a specific mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene where phenylalanine (F) at position 508 is deleted (Δ). This mutation leads to the production of a faulty CFTR protein, resulting in impaired chloride ion transport across cell membranes and causing the symptoms of cystic fibrosis.

Related Questions

Is cystic fibrosis chromosomal abnormality?

Yes, it is caused by a mutation in the gene for the protein CFTR.


What disease is called by a genetic mutation?

cystic fibrosis


Is cystic fibrosis a mutation?

yes, it is caused by a mutation in the gene cystic fibrosis transmembrane conductance regulator (CFTR). The most common mutation, which results in a loss of the amino acid phenylalanine


Is cystics fibrosis is caused by a mutation that is the dominant alle of a gene?

No, cystic fibrosis is an autosomal recessive disorder.


What kind of pathogen causes Cystic Fibrosis?

Cystic Fibrosis is caused by a genetic mutation in the CFTR gene. This mutation leads to the production of thick, sticky mucus in the lungs and other organs. It is not caused by a specific pathogen, but individuals with Cystic Fibrosis are more susceptible to respiratory infections.


Is Cystic Fibrosis a Germline mutation or an enviromental Mutation?

yes


True False Cystic fibrosis is caused by a mutation that is the dominant allele of a gene?

False. Cystic fibrosis is caused by a mutation in the CFTR gene, which is a recessive allele. An individual must inherit two copies of the mutated gene (one from each parent) to develop the condition.


Is cystic fibrosis caused by a virus?

No. Cystic fibrosis is a genetic disease.


What is the sequence of amino acid in cystic fibrosis?

The sequence of amino acids in cystic fibrosis is caused by a mutation in the CFTR gene, which leads to the production of a faulty cystic fibrosis transmembrane conductance regulator protein. This mutated protein results in abnormal function, leading to the characteristic symptoms of cystic fibrosis such as thick mucus production.


Where cystic fibrosis happens?

In the DNA: a mutation on chromosome 7


What term describes the inheritence cystic fibrosis?

The term that best describes the inheritance of cystic fibrosis is that it is genetic. Cystic fibrosis is caused by recessive alleles. Cystic fibrosis is an autosomal recessive genetic disease.


What chromosome does cystic fibrosis effect?

The gene on chromosome 7 produces a protein called cystic fibrosis trans-membrane regulator. Mutation in the DNA level of chromosome 7 leads to the absence of this protein which leads to cystic fibrosis. Cystic fibrosis is a recessive disease.