DRED
DRED IDNameOMIMRepeat UnitRepeat LocationGene
RD00049Spinocerebellar Ataxia 10603516ATTCTintronATXN10
RD00050Dystonia 3, Torsion, X-Linked314250CCCTCTintronTAF1
RD00051Myotonic Dystrophy 2602668CCTGintronCNBP
RD00052Fuchs Endothelial Corneal Dystrophy602272CTGintronTCF4
RD00053Duchenne Muscular Dystrophy300377GAAintronDMD
RD00054Friedreich Ataxia 1229300GAAintronFXN
RD00055Spinocerebellar Ataxia 36614153GGCCTGintronNOP56
RD00056Frontotemporal Degeneration and Amyotrophic Lateral Sclerosis105550GGGGCCintronC9orf72
RD00057Spinocerebellar Ataxia 31117210TGGAAintronBEAN1
RD00058Familial Adult Myoclonic Epilepsy-1601068TTTCA/TTTTAintronSAMD12
RD00059Epilepsy, Familial Adult Myoclonic, 2607876TTTCA/TTTTAintronSTARD7
RD00060Epilepsy, Familial Adult Myoclonic, 3613608TTTCA/TTTTAintronMARCHF6
RD00061Epilepsy, Familial Adult Myoclonic, 4615127TTTCA/TTTTAintronYEATS2
RD00062Epilepsy, Familial Adult Myoclonic, 6618074TTTCA/TTTTAintronTNRC6A
RD00063Epilepsy, Familial Adult Myoclonic, 7618075TTTCA/TTTTAintronRAPGEF2
RD00064Spinocerebellar Ataxia 37615945TTTCA/TTTTAintronDAB1

© 2024 Database of repeat expansion diseases.
Data collected by OmicsLab, IGDB, CAS. All rights reserved.

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