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Cell Type
- Embryonal Carcinoma
- Human Embryonic Stem (ES) Cells
- Human Induced Pluripotent Stem (iPS) Cells
- Modified Human ES Cells
- Modified Human iPS Cells
- Neural Stem Cells

Most Popular
- WA01
- WA09
- WA07
- iPS(IMR90)-4
- iPS-DF19-9-11T.H

Disease
- None Reported
- 16p11.2 disorders
- ABCA1 heterozygous
- Abetalipoproteinemia
- Alexander disease (Type II)
- Amyotrophic lateral sclerosis
- Arrhythmogenic Right Ventricular Cardiomyopathy
- Associated Pulmonary Arterial Hypertension status post and patent ductus arteriosus
- Associated Pulmonary Arterial Hypertension with Drugs and Toxins-Associated history
- Associated Pulmonary Arterial Hypertension with Eisenmenger's Syndrome
- Associated Pulmonary Arterial Hypertension with Lupus and pulmonary fibrosis
- Associated Pulmonary Arterial Hypertension with pulmonary veno-occlusive disease
- Associated Pulmonary Arterial Hypertension with ventricular septal defect and Eisenmenger's Syndrome
- Atrial Fibrillation
- Atrial Fibrillation|Coronary artery disease
- Atrial Fibrillation|Coronary artery disease|Interstitial Lung disease
- Atrial Fibrillation|Right Ventricular Outflow Tract Premature Ventricular Contractions
- Atrial Tachycardia
- Beta Thalassemia
- Carrier of Limb-Girdle Muscular Dystrophy
- Carrier of Spinal Muscular Atrophy (Type II)
- Carrier of X-linked Dystonia Parkinsonism
- Charcot-Marie-Tooth disease type 2A
- Choroideremia
- Chronic Myeloid Leukemia
- Congenital Heart Block
- Coronary artery disease
- Coronary artery disease|Myocardial infarction
- Danon disease
- Dilated Cardiomyopathy
- Down syndrome, Trisomy 21
- Duchenne Muscular Dystrophy
- EIF3F-associated Neurodevelopmental Disorder
- EIF3F-Related Neurodevelopmental Disorder
- Familial Alzheimer`s disease
- Familial Pulmonary Arterial Hypertension
- Familial Pulmonary Arterial Hypertension with Drugs and Toxins-Associated history
- Fragile X premutation
- Fragile X syndrome
- Fragile X syndrome|Autism
- Homozygous Familial Hypercholesterolemia
- Hyperalphalipoproteinemia
- Hypertrophic Cardiomyopathy
- Idiopathic Pulmonary Arterial Hypertension
- Inappropriate Sinus Tachycardia
- Klinefelter syndrome
- Left ventricular hypertrophy
- Left ventricular non-compaction
- Limb-Girdle Muscular Dystrophy, LGMD2B
- Mental illness
- Mild Left Ventricular Hypertrophy|Resolved Systolic Anterior Motion (of the mitral valve)
- Neuronal ceroid lipofuscinosis (Type II)
- None reported
- Nonseminomatous Germ Cell Tumor
- PACS1 (Schuurs-Hoeijmakers) syndrome
- PACS2 Syndrome
- Parkinson's disease
- Patau Syndrome
- Pulmonary Atresia
- Rett syndrome
- Right Ventricular Outflow Tract Premature Ventricular Contractions
- Severe Combined Immunodeficiency
- Sickle cell anemia SS
- Spinal Muscular Atrophy (Type I)
- Spinal Muscular Atrophy (Type II)
- Sporadic Alzheimer's disease
- Tangier disease
- Timothy Syndrome
- Turner Syndrome
- Ventricular tachycardia
- Ventricular tachycardia|Atrial Fibrillation|Long QT syndrome
- Ventricular tachycardia|Congenital Heart Block
- Ventricular tachycardia|Long QT syndrome
- Ventricular tachycardia|Long QT syndrome 2
- Ventricular tachycardia|Small Atrial Septal Defect
- X-linked Dystonia Parkinsonism

Age at Collection
- Adult
- Neonatal
- None Reported
- 0-10 Years
- 11-20 Years
- 21-30 Years
- 31-40 Years
- 41-50 Years
- 51-60 Years
- 61-70 Years
- 71-80 Years
- 81-90 Years
- 91-100 Years

Sex
- Female
- Male

Genetic Alteration/Mutation
- 47,XX,+21 (Trisomy 21)
- 47,XXY (Extra X chromosome)
- 47,XY,+21 (Trisomy 21)
- ABC1(K531N)het
- ABC1(K531N)het; ABC1(S2046R)het
- ABCA1
- ABCA1(R1210stop)het; ABCA1(intron 32,G[-25]C)het
- ADA
- ALK1
- APP (duplication)
- APPV717l mutation
- B2M
- BMPR2(R491W)
- CACNA1C
- CCR5
- DISC1 exon 8 wild-type mutation
- DJ1
- DYSF (heterozygous 1 mutation)
- DYSF (heterozygous 2 mutations)
- EIF3F
- ETV2
- FMR1
- FMR1 Knockout
- FMR1-FLAG
- GBA
- GFAP
- GFAP Corrected
- HBB
- HBB(E6V)
- HBB(E6V) Corrected
- KCNQ1
- KCTD13
- LDLR(del exon3-6)homo
- LDLR(del exon4-6)het
- LRRK2
- LRRK2
- MECP2
- MFN2
- MTP(R46G)
- MYH11
- PACS1
- PACS2
- SCN5A
- SMN1
- SNCA
- SNCA
- SOD1 > D90A
- SOD1 > D90A Corrected
- SR-BI
- TAF1 Variant
- TAF1 variant (hemizygous carrier)
- TAF1 Variant (heterozygous carrier)
- TAF1 variant (homozygous carrier)
- TAF1 Variant Corrected
- TPP1

Ethnicity
- None Reported
- African American
  - Nigerian
- African American|Asian
- African American|Latino
- Arab
- Asian
  - Chinese
  - Chinese|Caucasian
  - Filipino
  - Indian
  - Irani
  - Iraqi
  - Japanese
  - Japanese|Caucasian
  - Japanese|Caucasian > European
- Asian|Caucasian
- Asian|Latino
- Caucasian
  - European
  - European Asian > Indian
  - Nordic
- Caucasian
- Caucasian|Latino
  - North American
  - North American|Native American
- Caucasian|Native American
- Latino
  - North American
  - South American
- Latino|Native American
- Pacific Islander
- Unknown

Genetic Modification Keyword
- GFP (constitutive)
- Isogenic - Parkinson's Disease
- Isogenic - Parkinson's Disease
- Isogenic
  - Alexander disease (Type II)
  - Amyotrophic lateral sclerosis
  - Autism
  - Down syndrome, Trisomy 21
  - Fragile X syndrome
  - HIV
  - Immune rejection
  - Long QT syndrome
  - Neuronal ceroid lipofuscinosis (Type II)
  - Rett syndrome
  - schizophrenia
  - Sickle cell
  - Twin
  - X-linked Dystonia Parkinsonism
- N/A
- Reporter
  - Cardiac
  - Constitutive
  - Endothelial
  - Endothelial|Reporter; Hematopoetic
  - Neural
  - Self-renewal - Pluripotency
  - Vascular
  - Vascular - Smooth Muscle Cells

Provider
- Albert Einstein College of Medicine
- Allen Institute
  - Dr. Boaz Levi
- Biotrophix Pty.
  - Dr. Martin Pera
- Boston Children's Hospital
  - Dr. George Daley
- Boston University and Boston Medical Center's Center for Regenerative Medicine (CReM)
  - Dr. Steinberg, Dr. Mostoslavsky, Dr. Murphy
- Bresagen/Vertex
- Brigham and Women`s Hospital
  - Dr.Tracy Young-Pearse
- Brown University
  - Dr. Eric Morrow
- Buck Institute
- Cellartis/Takara
- Choroideremia Research Foundation
- EIF3F Research Foundation
- ESI/BioTime
- Fred Hutchinson Cancer Research Center
  - Dr. Beverly Torok-Storb
- Harvard Stem Cell Institute
  - Dr. Chad Cowan
- Jain Foundation
- Life Technologies
- Massachusetts General Hospital
- Medical College of Wisconsin
  - Dr. Ulrich Broeckel
- Morgridge Institute for Research
  - Dr. James Thomson
- PACS1 Foundation
- PACS2 Research Foundation
- Stanford University
  - Dr. Marlene Rabinovitch
  - Dr. Thomas Quertermous
- Technion
- The Johns Hopkins University
  - Dr. Elias Zambidis
  - Dr. Lewis Becker
- The Rockefeller University
  - Dr. Ali Brivanlou
- The Scripps Research Institute
  - Dr. Eric Topol
- University of California, Berkeley
- University of California, San Diego
  - Dr. Karl Willert
  - Dr. Kelly Frazer
  - Dr. Larry Goldstein
- University of California, San Francisco
- University of Luebeck
  - Dr. Christine Klein, Dr. Karen Gruetz, Dr. Philip Seibler
- University of Minnesota
  - Dr. Michael Kyba
- University of Pennsylvania
  - Dr. Daniel Rader
- University of Washington
  - Dr. Carol Ware
  - Dr. David Russell
- University of Wisconsin
  - Dr. Anita Bhattacharyya
  - Dr. Anita Bhattacharyya and Dr. Xinyu Zhao
  - Dr. Ei Terasawa
  - Dr. Igor Slukvin
  - Dr. James Thomson
  - Dr. John Svaren
  - Dr. Qiang Chang
  - Dr. Su-Chun Zhang
  - Dr. Timothy Kamp
- Whitehead Institute for Biomedical Research
- WiCell

Collection
- Alexander disease Collection
- Allen Institute Stem Cell Collection for Early Human Brain Development
- Alzheimer's disease
- Amyotrophic lateral sclerosis Collection
- Charcot-Marie-Tooth disease Collection
- Clinical Grade (cGMP) Cell Banks
- Down syndrome (Bhattacharyya) Collection
- Down syndrome (Russell) Collection
- Dysferlin-Deficient Collection
- Fragile X syndrome Collection
- Framingham Heart Study (FHS) Collection
- GENESIS Project Collection
- GeneSTAR Study Collection
- HyperGEN Study Collection
- National Stem Cell Bank (NSCB)
- Coronary artery disease and myocardial infarction (Dr. Eric Topol, Scripps Research Institute)
- Framingham Heart Study Collection (Dr. Chad Cowan, Harvard Stem Cell Institute)
- Insulin resistance syndrome (Dr. Thomas Quertermous, Stanford University)
- Left ventricular hypertrophy (Dr. Ulrich Broeckel, Medical College of Wisconsin)
- Lipid Conditions (Dr. Daniel Rader, University of Pennsylvania)
- Platelet Aggregation (Dr. Lewis Becker, The Johns Hopkins University)
- Pulmonary Artery Hypertension (Dr. Marlene Rabinovitch, Stanford University)
- QT Interval and ECG Cardiac Traits (Dr. Kelly Frazer, University of California San Diego)
- Sickle Cell Anemia (Dr. Steinberg, Dr. Mostoslavsky, Dr. Murphy, Boston University and Boston Medical Center's Center for Regenerative Medicine)
- NIH Approved
- PACS1 (Schuurs-Hoeijmakers) syndrome Collection
- Progenitor Cell Biology Consortium (PCBC) Collection
- Spinal Muscular Atrophy Collection
- Wellderly Study Collection
- X-linked Dystonia Parkinsonism
- iSCORE-PD: Isogenic Stem Cell Collection to Research Parkinson’s Disease

Tissue Origin
- Blood / PBMC
  - Blood
  - Blood (GM01715)
  - Blood (GM20920)
  - Peripheral Blood Mononuclear Cell
- Cord Blood
  - Umbilical Cord Blood CD34+ Cells
- Eye (Fibroblast)
  - Lens Fibroblast (GM09677)
- Lung (Fibroblast)
- Peripheral Blood Mononuclear Cells
- Skin (Fibroblast)
  - Fibroblast (GM00232)
  - Foreskin Fibroblast (HFF-1)
  - Skin Fibroblast
  - Skin Fibroblast (AG06872)
  - Skin Fibroblast (GM03813)
  - Skin Fibroblast (GM03814)
  - Skin Fibroblast (GM03815)
  - Skin Fibroblast (GM11270)
  - Skin Fibroblast (GM25383)
  - Skin Fibroblast (GM25393)
  - Skin Fibroblast (GM27159)
  - Skin Fibroblast (GM27160)
  - Skin Fibroblast Buttock (GM27161)
- Skin Fibroblast (GM07982)
- Testis

Reprogramming Method
- Non-Integrating - Episomal Plasmid
  - Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, cMyc, Bcl-xl)
  - Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, cMyc)
  - Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, L-Myc, Nanog, Lin28, SV40LT)
  - Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, L-Myc, shp53, Lin28)
  - Non-Integrating (Episomal plasmid: pEP4EO2SET2K (OCT4/SOX2/LT/KLF4), pEP4EO2SEN2K (OCT4/SOX2/NANOG/KLF4), and pCEP4-M2L (MYC/LIN28) plasmids)
- Non-Integrating - Sendai
  - Non-integrating (Sendai: Oct4, Klf4, Sox2, cMyc)
  - Sendai Virus (Oct4, Klf4, Sox2, Myc)
- Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, cMyc )
- Non-integrating (OCT4, SOX2, NANOG, LIN28, L-MYC, KLF4, SV40LT)
- Nucleofection
  - Transfection with a combination of pEP4EO2SET2K, pEP4EO2SEN2K and pCEP-M2L plasmids
- Viral Transfection
  - Viral transfection (Lentivirus: Oct4, Klf4, Sox2, cMyc)
  - Viral transfection (Lentivirus: Oct4, Sox2, Nanog, Lin28)
  - Viral Transfection (Retrovirus: Oct4, Klf4, Sox2, cMyc)

Cell Line	Cell Line Alias	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Ethnicity	Genetically Related Cell Lines	dbGaP Data
JFMD4	01458	Human iPS	Limb-Girdle Muscular Dystrophy, LGMD2B	c.879_883dupGACAG; p.Asp295GlyfsX45deletion of exon 52	Male	50 Years	Caucasian	No	No
JFMD5	01458	Human iPS	Limb-Girdle Muscular Dystrophy, LGMD2B	c.879_883dupGACAG; p.Asp295GlyfsX45deletion of exon 52	Male	50 Years	Caucasian	No	No
JFMD6	01458	Human iPS	Limb-Girdle Muscular Dystrophy, LGMD2B	c.879_883dupGACAG; p.Asp295GlyfsX45deletion of exon 52	Male	50 Years	Caucasian	No	No
JFNY1	JF25; 01456	Human iPS	Limb-Girdle Muscular Dystrophy, LGMD2B	c.5713C>T, p.Arg1905Xc.3517dupT, p.Ser1173PhefsX2	Male	32 Years	Asian	Yes	No
JFNY2	01456	Human iPS	Limb-Girdle Muscular Dystrophy, LGMD2B	c.5713C>T, p.Arg1905Xc.3517dupT, p.Ser1173PhefsX2	Male	32 Years	Asian	Yes	No
JFNY3	01456	Human iPS	Limb-Girdle Muscular Dystrophy, LGMD2B	c.5713C>T, p.Arg1905Xc.3517dupT, p.Ser1173PhefsX2	Male	32 Years	Asian	Yes	No
JFNY4	01456	Human iPS	Limb-Girdle Muscular Dystrophy, LGMD2B	c.5713C>T, p.Arg1905Xc.3517dupT, p.Ser1173PhefsX2	Male	32 Years	Asian	Yes	No
JFRBi1	01457	Human iPS	Limb-Girdle Muscular Dystrophy, LGMD2B	c.5946+1G>Ac.5497G>T; p.Glu1833X	Male	48 Years	Caucasian	No	No
JFRBi2	01457	Human iPS	Limb-Girdle Muscular Dystrophy, LGMD2B	c.5946+1G>Ac.5497G>T; p.Glu1833X	Male	48 Years	Caucasian	No	No
JFRBi3	01457	Human iPS	Limb-Girdle Muscular Dystrophy, LGMD2B	c.5946+1G>Ac.5497G>T; p.Glu1833X	Male	48 Years	Caucasian	No	No

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