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.

Pellegrini et al. BMC Bioinformatics 2012 13(Suppl 4):S3   doi:10.1186/1471-2105-13-S4-S3

Open Data