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  • Molecular assay reagents intended to identify CAG repeats in the ataxin 2 (ATXN2) gene, located at chromosome 12q24.1. A variation from the expected number of normal CAG trinucleotide repeat copies may produce altered DNA and improper gene functioning, resulting in full mutation. Normal alleles have 31 or fewer CAG trinucleotide repeats. Alleles with more than 32 CAG trinucleotide repeats have been associated with spinocerebellar ataxia type 2 (SCA2).
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