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Alagille syndrome is an inherited disorder; in which a person may have fewer than normal the number of small bile ducts inside the liver. Most people with Alagille have a defect in the JAG1(Jagged 1/drosophilia) gene that leds to Alagille syndrome. A child has a fifty percent chance of contraction Alagille syndrome from an affected parent.

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Which chromosomal mutation results in Alagille syndrome?

Alagille syndrome is typically caused by a deletion or mutation in the JAG1 gene located on chromosome 20. This gene provides instructions for making a protein involved in the development of various organs and tissues, including the liver, heart, and eyes.


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Related Questions

Chromosomal mutation resulting in alagille syndrome?

Alagille syndrome is predominately caused by changes in a gene called Jagged1 located on chromosome 20. The effects vary widely from severe Alagille syndrome, involving heart and liver disease, to others experiencing only minor manifestations.


What chromosomal mutation results in alagille syndrome?

translocation


Which chromosomal mutation results in Alagille syndrome?

Alagille syndrome is typically caused by a deletion or mutation in the JAG1 gene located on chromosome 20. This gene provides instructions for making a protein involved in the development of various organs and tissues, including the liver, heart, and eyes.


What is the type of mutation that causes Digeorge syndrome?

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What pathogen causes Down syndrome?

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