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

Table 1 Table of polyglutammine 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

Table of polyglutammine diseases. The table reports: disease code and full name, associated gene, ranges of healthy and pathogenic repeat numbers.

ISSN: 1471-2105