Multiple choice

The Huntington's disease mutation is genetically dominant, because either of a person's HTT genes being mutated causes the disease. CAG/CTG repeat expansions at the Huntington's disease is associated with which of the following genes?

  1. JPH3 gene

  2. ACSF3 gene

  3. ACD gene

  4. AMFR gene

  5. CYLD gene

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A Correct answer
Explanation

CAG/CTG repeat expansions at the Huntington's disease (HD)-like 2 locus have been identified in this gene, which is a member of the junctophilin gene family.