Cell line | Myotonic dystrophy | Fragile X* | ||
---|---|---|---|---|
Sequence (CTG) | Size (no. of repeats) | Sequence (CGG) | Size (no. of repeats) | |
HCT116+chr.3 was identical to HCT116 with the exception that the 11 CTG repeat allele was absent. | ||||
*All cells are male and therefore contain a single fragile X syndrome allele. | ||||
SW480 | Pure | 12/13 | 10+AGG+8+AGG+9 | 29 |
HCT116 | Pure | 11/12 | 9+AGG+1+AGG+19 | 31 |
LoVo | Pure | 10/12 | 19+AGGAGG+8 | 29 |