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Table 1 Table of polyglutammine diseases.

From: Tandem repeats discovery service (TReaDS) applied to finding novel cis-acting factors in repeat expansion diseases

Disease code Disease name Gene code Normal repeats Pathogenic repeats
DRPLA Dentatorubropallidoluysian atrophy ATN1 6 - 35 49 - 88
HD Huntington's disease HTT (Huntingtin) 10 - 35 35+
SBMA Kennedy disease (Spinobulbar muscular atrophy) HS-AR 9 - 36 38 - 62
SCA1 Spinocerebellar ataxia Type 1 ATXN1 6 - 35 49 - 88
SCA2 Spinocerebellar ataxia Type 2 ATXN2 14 - 32 33 - 77
SCA6 Spinocerebellar ataxia Type 6 CACNA1A 4 - 18 21 - 30
SCA7 Spinocerebellar ataxia Type 7 ATXN7 7 - 17 38 - 120
SCA17 Spinocerebellar ataxia Type 17 TBP 25 - 42 47 - 63
SCA3 Machado-Joseph disease (Spinocerebellar ataxia Type 3) ATXN3 12 - 40 55 - 86
  1. Table of polyglutammine diseases. The table reports: disease code and full name, associated gene, ranges of healthy and pathogenic repeat numbers.