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Tay Sachs disease is an autosomal recessive disorder involving the hexoaminidase gene. What type of mutation occurs in this gene?

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05-02-2021
Biology

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WILL GIVE BRAIINLIEST

Tay Sachs disease is an autosomal recessive disorder involving the hexoaminidase gene. What type of mutation occurs in this gene?

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Fkwochcndndidn Fkwochcndndidn · Answer 1 · 2021-02-05T12:50:01-05:00

Fkwochcndndidn Fkwochcndndidn

05-02-2021

Tay-Sachs disease is caused by mutations in the HEXA gene and inheritance is autosomal recessive . The HEXA gene gives the body instructions to make part of the beta-hexosaminidase A enzyme, which is needed to break down a substance called GM2 ganglioside.

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Samanthasummers12013idn Samanthasummers12013idn · Answer 2 · 2021-02-05T12:50:02-05:00

Samanthasummers12013idn Samanthasummers12013idn

05-02-2021

Answer:

Frameshift mutation

Explanation:

A frameshift mutation is a genetic mutation caused by insertions or deletions that shift the whole sequence.

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