iPSC細胞庫(一覽表) |
Ø iPSC聯盟提供研究等級之無疾病或有疾病的人類誘導幹細胞給一般大眾及產業界做使用。
Ø 本設施之細胞庫在Dr. Wataru Fujibuchi團隊 (CiRA, University of Kyoto)所創造之Stemcell Knowledge & Information Portal (SKIP)中排名第五。SKIP是一個提供全球細胞庫及幹細胞相關研究資訊的幹細胞資料庫。詳情請見: https://skip.stemcellinformatics.org/en/
Ø
本聯盟僅授權BCRC細胞庫為唯一合法分讓渠道，敬請各位使用者購買時注意細胞來源
Ø 請點選表格最右側連結至BCRC細胞庫網站進行購買及閱覽細胞株詳細資訊(如鑑定結果、培養條件等)。
Ø 聯盟亦提供iPSC產製服務，更多資訊請洽聯盟聯絡窗口。
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Donor Status
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Donor Status in Chinese
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iPSC Clone Number
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Note
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Gender
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Age
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Donor Cells
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Mutations
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Purchase
Links
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Purchase
Links
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Feeder-Dependent
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Feeder-Free
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||||||||
Normal Lines
|
無已知疾病之健康捐贈者
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IBMS-iPSC-001-02
|
---
|
F
|
33
|
PBMCs
|
---
|
||
IBMS-iPSC-002-07
|
---
|
M
|
22
|
PBMCs
|
---
|
||||
IBMC-iPSC-003-06
|
---
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F
|
31
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PBMCs
|
---
|
||||
IBMS-iPSC-004-02
|
---
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M
|
32
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PBMCs
|
---
|
||||
NTUH-iPSC-001-05
|
---
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F
|
45
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PBMCs
|
---
|
||||
NTUH-iPSC-002-02
|
---
|
M
|
52
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PBMCs
|
---
|
||||
TVGH-iPSC-001-04
|
---
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F
|
25
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PBMCs
|
---
|
||||
TVGH-iPSC-002-07
|
---
|
M
|
26
|
PBMCs
|
---
|
||||
FIRDI-iPSC-002-30
|
---
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M
|
39
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PBMCs
|
---
|
||||
NHRI-iPSC-001-01
|
---
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M
|
27
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PBMCs
|
---
|
||||
Polycystic Kidney Disease (PKD)
|
多囊性腎臟病
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IBMS-iPSC-012-012
|
---
|
M
|
35
|
PBMCs
|
Chr16:
2160801_2delTC (p.Ser1457fs)
|
||
IBMS-iPSC-013-07
|
---
|
M
|
36
|
PBMCs
|
Chr16:
2166843 C>T
|
||||
IBMS-iPSC-014-05
|
---
|
F
|
63
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PBMCs
|
PKD2/R803X,
Chr4: 88989098 C>T
|
||||
Atrial
Fibrillation (AF)
|
心房顫動
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IBMS-iPSC-015-06
|
---
|
M
|
53
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PBMCs
|
---
|
---
|
|
IBMS-iPSC-016-06
|
---
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M
|
34
|
PBMCs
|
---
|
---
|
|||
IBMS-iPSC-017-02
|
---
|
F
|
32
|
PBMCs
|
---
|
---
|
|||
Parkinson's Disease (PD)
|
帕金森氏症
|
IBMS-iPSC-018-09
|
---
|
M
|
44
|
PBMCs
|
LRRK2 p.
G2385R rs34778348 /chromosome 12q12
|
---
|
|
IBMS-iPSC-019-11
|
---
|
F
|
67
|
PBMCs
|
Heterozygous LRRK2 p. I2012T rs34015634 /chromosome
12q12
|
||||
IBMS-iPSC-020-01
|
---
|
M
|
53
|
PBMCs
|
LRRK2 p.
G2385R rs34778348 /chromosome 12q12
|
||||
IBMS-iPSC-042-01
|
---
|
F
|
60
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PBMCs
|
LRRK2 p. I1371V
|
---
|
|||
IBMS-iPSC-043-05
|
---
|
F
|
32
|
PBMCs
|
PLA2G6
C.G991T (p. D331Y)
|
---
|
|||
ALDH2
mutation
|
乙醛脫氫酶突變
|
IBMS-iPSC-021-04
|
---
|
M
|
47
|
PBMCs
|
ALDH2 rs671 G>A p.Glu504Lys
|
---
|
|
IBMS-iPSC-022-01
|
---
|
M
|
57
|
PBMCs
|
ALDH2 rs671 G>A p.Glu504Lys
|
---
|
|||
IBMS-iPSC-023-03
|
---
|
F
|
74
|
PBMCs
|
ALDH2 rs671 G>A p.Glu504Lys
|
---
|
|||
Fabry Disease
|
法布瑞氏症
|
IBMS-iPSC-024-03
|
---
|
M
|
28
|
PBMCs
|
p.
E398DfsX6
|
---
|
|
IBMS-iPSC-025-03
|
---
|
M
|
66
|
PBMCs
|
IVS4+919G>A
|
||||
IBMS-iPSC-026-02
|
---
|
M
|
67
|
PBMCs
|
IVS4+919G>A
|
---
|
|||
Aromatic L-Amino Acid Decarboxylase Deficiency (AADC)
|
芳香族L-胺基酸類脫羧基酶缺乏症
|
IBMS-iPSC-027-01
|
---
|
M
|
11
|
PBMCs
|
IVS6+4/IVS6+4
|
---
|
|
IBMS-iPSC-028-01
|
---
|
M
|
41
|
PBMCs
|
IVS6+4/WT
|
---
|
|||
IBMS-iPSC-029-01
|
---
|
F
|
10
|
PBMCs
|
IVS6+4/IVS6+4
|
||||
Mitochondrial DNA mutation
|
粒線體DNA突變
|
IBMS-iPSC-030-06
|
Sensorineural Hearing Loss
|
F
|
39
|
PBMCs
|
MTRNR1,
mtDNA1555A>G (A: 15.3%, G: 84.7%)
|
||
IBMS-iPSC-031-05
|
Deafness
|
F
|
40
|
Fibroblasts
|
A8344G mutation in the mitochondrial tRNALys
gene (A: 70.2%, G: 29.8%)
|
||||
TVGH-iPSC-025-06
|
---
|
M
|
28
|
Fibroblasts
|
A3243G transition
in mitochondrial DNA
|
---
|
|||
TVGH-iPSC-026-11
|
---
|
M
|
32
|
Fibroblasts
|
A3243G transition
in mitochondrial DNA
|
---
|
|||
Sialidosis Disease
|
涎酸酵素缺乏症
|
IBMS-iPSC-033-02
|
---
|
F
|
16
|
PBMCs
|
NEU1/chromosome
6p21.33, A544G mutation (Exon3 p.Ser182Gly) and 667-679 deletion (Exon4)
|
||
Short QT syndrome (SQTS)
|
短QT综合症
|
IBMS-iPSC-044-05
|
---
|
F
|
65
|
PBMCs
|
SCN3A
|
---
|
|
IBMS-iPSC-045-02
|
---
|
M
|
81
|
PBMCs
|
DSP g.
Chr6: 7585411G>A | c. 7916G>A | p. R2639Q
|
---
|
|||
Huntington's
Disease (HD)
|
亨丁頓舞蹈症
|
IBMS-iPSC-053-02
|
---
|
F
|
60
|
PBMCs
|
---
|
---
|
|
IBMS-iPSC-053-05
|
---
|
F
|
60
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PBMCs
|
---
|
---
|
|||
Premature Ovarian Failure (POF)
|
卵巢早衰症
|
NTUH-iPSC-003-40
|
Turner syndrome
|
F
|
32
|
PBMCs
|
---
|
---
|
|
NTUH-iPSC-004-06
|
Turner syndrome
|
F
|
34
|
PBMCs
|
---
|
---
|
|||
NTUH-iPSC-005-02
|
---
|
F
|
33
|
PBMCs
|
---
|
---
|
|||
Familial Amyloid Neuropathy (FAP)
|
家族性類澱粉多發性神經病變
|
NTUH-iPSC-007-03
|
---
|
M
|
64
|
PBMCs
|
---
|
---
|
|
NTUH-iPSC-008-11
|
---
|
M
|
61
|
PBMCs
|
---
|
---
|
|||
NTUH-iPSC-009-07
|
---
|
F
|
77
|
PBMCs
|
---
|
---
|
|||
Type 1 Diabetes
|
第1型糖尿病
|
NTUH-iPSC-010-06
|
---
|
F
|
33
|
PBMCs
|
---
|
---
|
|
NTUH-iPSC-011-05
|
---
|
F
|
51
|
PBMCs
|
---
|
---
|
|||
NTUH-iPSC-012-04
|
---
|
M
|
26
|
PBMCs
|
---
|
---
|
|||
Prader-Willi Syndrome (PWS)
|
普瑞德威利症候群 (小胖威利)
|
NTUH-iPSC-013-01
|
---
|
F
|
11
|
PBMCs
|
---
|
---
|
|
NTUH-iPSC-014-01
|
---
|
F
|
5
|
PBMCs
|
---
|
---
|
|||
Spinocerebellar Ataxia (SCA)
|
脊髓小腦萎縮症
|
TVGH-iPSC-003-12
|
SCA3
|
M
|
37
|
PBMCs
|
---
|
---
|
|
TVGH-iPSC-004-13
|
SCA36
|
F
|
58
|
PBMCs
|
---
|
---
|
|||
TVGH-iPSC-005-05
|
SCA36
|
M
|
64
|
PBMCs
|
---
|
---
|
|||
IBMS-iPSC-046-06
|
SCA22
|
F
|
62
|
PBMCs
|
c.
679_681delTTC
|
---
|
|||
IBMS-iPSC-047-03
|
SCA22
|
F
|
52
|
PBMCs
|
c.
679_681delTTC
|
---
|
|||
IBMS-iPSC-050-04
|
SCA3
|
F
|
46
|
PBMCs
|
---
|
---
|
|||
IBMS-iPSC-050-05
|
SCA3
|
F
|
46
|
PBMCs
|
---
|
---
|
|||
IBMS-iPSC-051-02
|
SCA2
|
F
|
47
|
PBMCs
|
---
|
---
|
|||
IBMS-iPSC-051-05
|
SCA2
|
F
|
47
|
PBMCs
|
---
|
---
|
|||
IBMS-iPSC-052-01
|
SCA2
|
M
|
61
|
PBMCs
|
---
|
---
|
|||
Leber's Hereditary Optic Neuropathy (LHON)
|
雷伯氏遺傳性視神經病變
|
TVGH-iPSC-006-06
|
---
|
M
|
47
|
PBMCs
|
---
|
---
|
|
TVGH-iPSC-007-08
|
---
|
F
|
42
|
PBMCs
|
---
|
---
|
|||
TVGH-iPSC-010-09
|
---
|
F
|
61
|
PBMCs
|
Mitochondrial MT-ND4 gene/m.11778G > A (A:95.71%, G:4.29%)
|
---
|
|||
Juvenile Macular Degeneration (JMD)
|
青少年黄斑部病變
|
TVGH-iPSC-012-04
|
Best Dystrophy
|
M
|
11
|
PBMCs
|
(BEST1
(VMD2)) 11q12.3
|
---
|
|
TVGH-iPSC-013-05
|
X-linked Juvenile Retinoschisis
|
M
|
16
|
PBMCs
|
g.488G > A mutation of RS1 gene, p.W163X
|
---
|
|||
TVGH-iPSC-014-05
|
---
|
M
|
13
|
PBMCs
|
---
|
---
|
|||
Facioscapulohumeral Muscular Dystrophy (FSHD)
|
顏面肩胛肱骨型肌肉失養症
|
TVGH-iPSC-019-07
|
---
|
M
|
21
|
PBMCs
|
---
|
---
|
|
TVGH-iPSC-020-10
|
---
|
M
|
55
|
PBMCs
|
---
|
---
|
|||
TVGH-iPSC-024-42
|
---
|
M
|
22
|
PBMCs
|
---
|
---
|
|||
Monogenic Diabetes
|
單基因糖尿病
|
TVGH-iPSC-015-16
|
---
|
M
|
13
|
PBMCs
|
---
|
---
|
|
TVGH-iPSC-016-01
|
---
|
M
|
11
|
PBMCs
|
---
|
---
|
|||
TVGH-iPSC-017-08
|
---
|
F
|
14
|
PBMCs
|
---
|
---
|
|||
Frontotemporal Dementia (FTD)
|
額顳葉型失智症
|
TVGH-iPSC-021-10
|
---
|
F
|
64
|
PBMCs
|
---
|
---
|
|
TVGH-iPSC-022-04
|
---
|
F
|
57 |
PBMCs
|
---
|
---
|
|||
TVGH-iPSC-023-02
|
---
|
F
|
54
|
PBMCs
|
---
|
---
|
|||
Schizophrenia
|
思覺失調症
|
NHRI-iPSC-003-04
|
---
|
M
|
64
|
PBMCs
|
---
|
---
|
|
NHRI-iPSC-004-03
|
---
|
F
|
61
|
PBMCs
|
---
|
---
|
|||
NHRI-iPSC-005-01
|
---
|
F
|
42
|
PBMCs
|
---
|
---
|
|||
NHRI-iPSC-006-01
|
---
|
F
|
57
|
PBMCs
|
---
|
---
|
|||
NHRI-iPSC-007-01
|
---
|
M
|
25
|
PBMCs
|
---
|
---
|
|||
NHRI-iPSC-008-01
|
---
|
M
|
25
|
PBMCs
|
---
|
---
|
|||
Bardet-Biedl Syndrome |
巴德-畢德氏症候群
|
IBMS-iPSC-063-06
|
---
|
M |
37
|
PBMCs
|
C534+1G>T |
---
|
|
Motor Neuron Disease (ALS)
|
運動神經元疾病(漸凍症)
|
IBMS-iPSC-068-02
|
---
|
M
|
53
|
PBMCs
|
---
|
---
|
|
IBMS-iPSC-069-05 |
--- |
M
|
75 |
PBMCs
|
---
|
---
|
|||
Catecholaminergic polymorphic ventricular tachycardia (CPVT) |
兒茶酚胺多型性心室頻脈
|
IBMS-iPSC-075-01 |
---
|
M |
47 |
PBMCs
|
RYR2 |
---
|
|
Pantothenate Kinase-Associated Neurodegeneration (PKAN) |
泛酸鹽激酶關聯之神經退化性疾病 |
IBMS-iPSC-082-01 |
---
|
M
|
15 |
PBMCs
|
PANK2 |
---
|
|
IBMS-iPSC-084-06 |
--- |
M
|
9 |
PBMCs
|
PANK2 |
---
|