| Name / ID | Type | Disease | RRID | Causal gene(s) | Mutation | Originating lab |
|---|---|---|---|---|---|---|
| MUSli004-A | Cell Lines | SCA3 | CVCL_VN11 |
ATXN3 | ? | Faculty of Medicine Siriraj Hospital (MUSI) |
| Nes1g FLAG/FLAG | Mouse Models | SCAR8/ARCA1 | — |
SYNE1 | KASH reporter' mouse model | Washington University School of Medicine |
| Nes1g STOP/STOP | Mouse Models | SCAR8/ARCA1 | — |
SYNE1 | Depletion of giant isoforms of Nesprin1 | Washington University School of Medicine |
| NIMHi026-A | Cell Lines | MSA/OPCA | — |
? | — | National Institute of Mental Health and Neurosciences (NIMH) |
| NIMHi028-A | Cell Lines | MSA/OPCA | — |
? | — | National Institute of Mental Health and Neurosciences (NIMH) |
| NOP56-(TG3C2)62 | Mouse Models | SCA36 | — |
NOP56 | AAV9 with human NOP56 (TG3C2)62 | Mayo Clinic |
| NYSCF-AD-1000-ASC2-Dura-SV-iPSC1 | Cell Lines | MSA/OPCA | CVCL_AD05 |
? | — | New York Stem Cell Foundation Research Institute |
| NYSCF-AD-1000-ASC2-Skin-SV-iPSC1 | Cell Lines | MSA/OPCA | CVCL_AD06 |
? | — | New York Stem Cell Foundation Research Institute |
| Olig001-SYN mouse model | Mouse Models | MSA/OPCA | — |
Sporadic | AAV overexpressing α-synuclein | University of Alabama at Birmingham |
| P1 | Cell Lines | AOA1 | — |
APTX | pW279X/pW279X | Columbia University College of Physicians and Surgeons |
| P1 (MSA-P) | Cell Lines | MSA/OPCA | — |
? | — | University of Milan |
| P1027 | Cell Lines | AOA1 | — |
APTX | pW279X/pW279X | Istituto Neurologico Carlo Besta |
| P1028 | Cell Lines | AOA1 | — |
APTX | pW279X/pW279X | Istituto Neurologico Carlo Besta |
| P1619 | Cell Lines | AOA1 | — |
APTX | pW279X/pW279X | Istituto Neurologico Carlo Besta |
| P1657 | Cell Lines | AOA1 | — |
APTX | pR306X/pR306X | Istituto Neurologico Carlo Besta |
| P2 | Cell Lines | AOA1 | — |
APTX | pW279X/pW279X | Columbia University College of Physicians and Surgeons |
| P2 (MSA-P) | Cell Lines | MSA/OPCA | — |
? | — | University of Milan |
| P3 | Cell Lines | AOA1 | — |
APTX | pW279X/* | Columbia University College of Physicians and Surgeons |
| P980 | Cell Lines | AOA1 | — |
APTX | pW279X/pW279X | Istituto Neurologico Carlo Besta |
| Pa1-SCA3 | Cell Lines | SCA3 | — |
ATXN3 | 80 CAG | Chinese Academy of Sciences |
| Pa2-SCA3 | Cell Lines | SCA3 | — |
ATXN3 | 78 CAG | Chinese Academy of Sciences |
| Patient 1 | Cell Lines | SPG7 | — |
SPG7 | c.1449 + 1G > A (exon 10) and c.1529C>T (exon 11) | University of Sydney |
| Patient 1 (MSA-P) | Cell Lines | MSA/OPCA | — |
GGC expansion in NOTCH2NLC | 112-138 GGC | First Affiliated Hospital of Nanchang University |
| Patient 2 | Cell Lines | SPG7 | — |
SPG7 | c.415C > T (exon 4) and c.941T>A (exon 7) | University of Sydney |
| Patient 3 | Cell Lines | SPG7 | — |
SPG7 | chr16:g.89623293A > G, c.2182-2A > G (intron 16- exon 17) and c.1529C>T (exon 11) | University of Sydney |
| Patient 4 (MSA-C) | Cell Lines | MSA/OPCA | — |
GGC expansion in NOTCH2NLC | 101-126 GGC | First Affiliated Hospital of Nanchang University |
| Patient line 1 | Cell Lines | SACS/ARSACS/SPAX6 | — |
SACS | c.8339T>C (p.Phe2780Cys) and c.12416T>C (p.Leu4139Ser)/c.11675C>G (p.Ser3892X) (sibling from patient line 2) | UCL Queen Square Institute of Neurology |
| Patient line 2 | Cell Lines | SACS/ARSACS/SPAX6 | — |
SACS | c.8339T>C (p.Phe2780Cys) and c.12416T>C (p.Leu4139Ser)/c.11675C>G (p.Ser3892X) (sibling from patient line 1) | UCL Queen Square Institute of Neurology |
| Patient P1 | Cell Lines | SCA27B | — |
FGF14 | 295/304 GAA-TTC | McGill University |
| Patient P1 hiPSC clone 4 | Cell Lines | SCA27B | — |
FGF14 | 293/303 GAA-TTC | McGill University |
| Patient P1 hiPSC clone 5 | Cell Lines | SCA27B | — |
FGF14 | 295/304 GAA-TTC | McGill University |
| Patient P1 hiPSC clone 6 | Cell Lines | SCA27B | — |
FGF14 | 291/315 GAA-TTC | McGill University |
| Patient P8 | Cell Lines | SCA27B | — |
FGF14 | 9/518 GAA-TTC | McGill University |
| Patient P8 hiPSC clone 1 | Cell Lines | SCA27B | — |
FGF14 | 9/597 GAA-TTC | McGill University |
| Patient P8 hiPSC clone 2 | Cell Lines | SCA27B | — |
FGF14 | 9/607 GAA-TTC | McGill University |
| Patient P8 hiPSC clone 3 | Cell Lines | SCA27B | — |
FGF14 | 9/527 GAA-TTC | McGill University |
| Patient P8 hiPSC clone 5 | Cell Lines | SCA27B | — |
FGF14 | 9/525 GAA-TTC | McGill University |
| Patient P9 | Cell Lines | SCA27B | — |
FGF14 | 16/409 GAA-TTC | McGill University |
| Patient P9 hiPSC clone 1 | Cell Lines | SCA27B | — |
FGF14 | 16/402 GAA-TTC | McGill University |
| Patient P9 hiPSC clone 2.1 | Cell Lines | SCA27B | — |
FGF14 | 16/411 GAA-TTC | McGill University |
| Patient P9 hiPSC clone 2.2 | Cell Lines | SCA27B | — |
FGF14 | 16/390 GAA-TTC | McGill University |
| Patient P9 hiPSC clone 4 | Cell Lines | SCA27B | — |
FGF14 | 16/402 GAA-TTC | McGill University |
| PDGF-ß-EGFP-α-Syn transgenic mouse | Mouse Models | MSA/OPCA | — |
Sporadic | expressing a stable enhanced green fluorescent protein (eGFP) tagged in the C-terminal site of a human (h)α-synuclein construct | University of California |
| PDGF-ß-α-Syn transgenic mouse | Mouse Models | MSA/OPCA | — |
Sporadic | human α-synuclein cDNA | University of California |
| PLP-α-Syn transgenic mouse | Mouse Models | MSA/OPCA | MGI:3,604,008 |
Sporadic | Overexpression of human wild-type α-syn | Ludwig Maximilians University |
| Plp1-tTA::tetO-SNCA*A53T bi-transgenic mice | Mouse Models | MSA/OPCA | — |
Sporadic | mutant A53T human α-syn specifically in oligodendrocytes | Kyushu University |
| PN1 | Cell Lines | SACS/ARSACS/SPAX6 | — |
SACS | p.[(Arg3636Gln;Pro3652Thr)];[Leu3745fsTer1] | University of Milan |
| PN2 | Cell Lines | SACS/ARSACS/SPAX6 | — |
SACS | p.[Cys72fsTer4];[(Arg3636Gln;Pro3652Thr)] | University of Milan |
| PN3 | Cell Lines | SACS/ARSACS/SPAX6 | — |
SACS | p.[Glu723fsTer15];[Phe3209fsTer46] | University of Milan |
| PN4 | Cell Lines | SACS/ARSACS/SPAX6 | — |
SACS | p.[Leu2374Ser];[deleted_allele] | University of Milan |
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