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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 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
- 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
- None reported
- Nonseminomatous Germ Cell Tumor
- PACS1 (Schuurs-Hoeijmakers) syndrome
- PACS2 Syndrome
- Parkinson's disease
- Parkinson's disease
- Parkinson's Disease
- Patau Syndrome
- PTEN Hamartoma Tumor Syndrome (PHTS)
- 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)
- Spinal Muscular Atrophy (Type II) > Carrier of Spinal Muscular Atrophy (Type II)
- Sporadic Alzheimer's disease
- Tangier disease
- Timothy Syndrome
- Tuberous Sclerosis Complex
- Tuberous Sclerosis Complex
- 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
- DNAJC6
- DYSF (heterozygous 1 mutation)
- DYSF (heterozygous 2 mutations)
- EIF3F
- ETV2
- FBX07
- 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
- PHTS (heterozygous)
- PHTS (homozygous)
- PHTS (isogenic control)
- PINK1
- PRKN
- PRKN
- 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
- TSC2 (heterozygous)
- TSC2 (homozygous)
- TSC2 (homozygous)
- TSC2 Corrected

Ethnicity
- None Reported
- African American
  - African American|Asian
  - African American|Latino
  - Nigerian
- Arab
- Asian
  - Asian|Caucasian
  - Asian|Latino
  - Chinese
  - Chinese|Caucasian
  - Filipino
  - Indian
  - Irani
  - Iraqi
  - Japanese
  - Japanese|Caucasian
  - Japanese|Caucasian > European
- Caucasian
- 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 - PTEN Hamartoma Tumor Syndrome (PHTS)
- Isogenic - Tuberous Sclerosis Complex
- Isogenic - Tuberous Sclerosis Complex
- 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)
  - PTEN Hamartoma Tumor Syndrome (PHTS)
  - 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. Elizabeth Buttermore
  - 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 Michael J. Fox Foundation for Parkinson’s Research
- 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 Gomez
  - 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
- Parkinson’s LRRK2 iPSC Cell Line Collection
- PTEN Hamartoma Tumor Syndrome (PHTS) Collection
- Tuberous Sclerosis Complex Collection

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 Cell
- Peripheral Blood Mononuclear Cell
- Skin (Fibroblast)
  - Fibroblast (GM00232)
  - Foreskin Fibroblast (HFF-1)
  - Skin Fibroblast
  - Skin Fibroblast (AG06872)
  - Skin Fibroblast (GM03813)
  - Skin Fibroblast (GM03814)
  - Skin Fibroblast (GM03815)
  - Skin Fibroblast (GM07982)
  - Skin Fibroblast (GM11270)
  - Skin Fibroblast (GM25383)
  - Skin Fibroblast (GM25393)
  - Skin Fibroblast (GM27159)
  - Skin Fibroblast (GM27160)
  - Skin Fibroblast Buttock (GM27161)
- Skin Fibroblast
- 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)
  - Non-Integrating (Sendai: Oct4, Klf4, Sox2, cMyc)
  - Sendai Virus (Oct4, Klf4, Sox2, Myc)
- Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, cMyc )
- Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, L-Myc)
- Non-integrating (OCT4, SOX2, NANOG, LIN28, L-MYC, KLF4, SV40LT)
- Non-Integrating (Sendai: Oct4, Klf4, Sox2, cMyc
- Non-Integrating (Sendai: Oct4, Klf4, Sox2, cMyc)
- Non-integrating (Sendai: Oct4, Klf4, Sox2, cMyc)
- Non-Integrating (Sendai: Oct4, Klf4, Sox2, cMyc)
- 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
SUSL-046_C9		Human iPS	Parkinson's Disease	LRRK2, p.G2019S Homozygous	Male	65 years	Caucasian	No	No
SUSL-066_C2		Human iPS	Parkinson's Disease	LRRK2, p.G2019S, Heterozygous	Male	74 years	Caucasian	No	No
SUSL-066_C5		Human iPS	Parkinson's Disease	LRRK2, p.G2019S, Heterozygous	Male	74 years	Caucasian	No	No
TE03	I3	Human ES	None reported		Female			No	No
TE04	I4	Human ES	None reported		Female			No	No
TE06	I6	Human ES	None reported		Male			No	No
UC06	HSF-6	Human ES	None reported		Female			No	No
UCSD001i-5-1	iPSCORE_5_1	Human iPS	None reported		Female	43 Years	Caucasian > European	Yes	Yes
UCSD002i-16-1	iPSCORE_16_1	Human iPS	None reported		Male	51 Years	Asian > Indian	Yes	Yes
UCSD003i-16-2	iPSCORE_16_2	Human iPS	None reported		Female	47 Years	Asian > Indian	Yes	Yes

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