1. Angelman syndrome |
UBE3A-ATS |
Antisense transcription |
[37] |
2. Prader-willi syndrome |
sno-lncRNAs |
Splicing regulation |
[40] |
3. Beckwith-Wiedemann syndrome |
KCNQ1OT1 |
Recruitment of chromatin-modifying complexes |
[36]; [59] |
4. Silver-Russell syndrome |
H19 |
Recruitment of chromatin-modifying complexes; miRNA dependent mechanism |
[51–58] |
5.Pseudohypoparathyroidism type 1b |
A\S-1 |
Antisense transcription |
[63, 64] |
|
A\B |
Antisense transcription |
[61, 62] |
6. Alzheimer disease |
BACE1-AS |
RNA-RNA duplex formation |
[45] |
|
LPR1-AS |
Recruitment of chromatin-modifying complexes |
[68] |
|
51А |
Splicing regulation |
[42] |
|
17А |
Splicing regulation |
[73] |
|
ciRS −7 |
miRNA dependent mechanism |
[75–77] |
7. Huntington disease |
HTTAS |
miRNA dependent mechanism |
[79] |
8. Spinocerebellar ataxia type 7 |
SCAANT1 |
Antisense transcription |
[39] |
|
lnc-SCA7 |
miRNA dependent mechanism |
[83] |
9. Spinocerebellar ataxia type 8 |
ATXN8OS |
Splicing regulation |
[41] |
10. Facioscapulohumeral muscular dystrophy |
DBE-T |
Recruitment of chromatin-modifying complexes |
[36] |
11. Spinal muscular atrophy |
SMN-AS1 |
Recruitment of chromatin-modifying complexes |
[97] |
12. Alpha thalassemia |
LUC7 |
Antisense transcription |
[99] |
13. Opitz-Kaveggia syndrome |
ncRNA-a |
Recruitment of chromatin-modifying complexes |
[102] |
14. Hirschsprung disease |
cir-ZNF609 |
miRNA dependent mechanism |
[43] |
15. Cartilage-hair hypoplasia |
RMRP |
miRNA dependent mechanism |
[44] |