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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
- Timothy Syndrome
- 16p11.2 disorders
- Sickle cell anemia SS
- Beta Thalassemia
- Choroideremia
- Neuronal ceroid lipofuscinosis (Type II)
- Nonseminomatous Germ Cell Tumor
- Alexander disease (Type II)
- Down syndrome, Trisomy 21
- Familial Alzheimer`s disease
- Chronic Myeloid Leukemia
- Severe Combined Immunodeficiency
- Reticulosis
- Carrier of Limb-Girdle Muscular Dystrophy
- Limb-Girdle Muscular Dystrophy, LGMD2B
- X-linked Dystonia Parkinsonism
- Carrier of X-linked Dystonia Parkinsonism
- Left ventricular hypertrophy
- PACS1 (Schuurs-Hoeijmakers) syndrome
- PACS2 syndrome
- Homozygous Familial Hypercholesterolemia
- ABCA1 heterozygous
- Tangier disease
- Abetalipoproteinemia
- Hyperalphalipoproteinemia
- Patau Syndrome
- Coronary artery disease|Myocardial infarction
- Coronary artery disease
- Turner Syndrome
- Idiopathic Pulmonary Arterial Hypertension
- Associated Pulmonary Arterial Hypertension with Drugs and Toxins-Associated history
- Familial Pulmonary Arterial Hypertension
- Associated Pulmonary Arterial Hypertension with pulmonary veno-occlusive disease
- Associated Pulmonary Arterial Hypertension with ventricular septal defect and Eisenmenger's Syndrome
- Associated Pulmonary Arterial Hypertension with Lupus and pulmonary fibrosis
- Associated Pulmonary Arterial Hypertension status post and patent ductus arteriosus
- Associated Pulmonary Arterial Hypertension with Eisenmenger's Syndrome
- Familial Pulmonary Arterial Hypertension with Drugs and Toxins-Associated history
- Hypertrophic Cardiomyopathy
- Left ventricular non-compaction
- Danon disease
- Dilated Cardiomyopathy
- Ventricular tachycardia|Small Atrial Septal Defect
- Atrial Fibrillation
- Ventricular tachycardia|Atrial Fibrillation|Long QT syndrome
- Atrial Fibrillation|Right Ventricular Outflow Tract Premature Ventricular Contractions
- Atrial Fibrillation|Coronary artery disease|Interstitial Lung disease
- Arrhythmogenic Right Ventricular Cardiomyopathy
- Mild Left Ventricular Hypertrophy|Resolved Systolic Anterior Motion (of the mitral valve)
- Right Ventricular Outflow Tract Premature Ventricular Contractions
- Duchenne Muscular Dystrophy
- Ventricular tachycardia
- Ventricular tachycardia|Long QT syndrome
- Ventricular tachycardia|Long QT syndrome 2
- Pulmonary Atresia
- Inappropriate Sinus Tachycardia
- Ventricular tachycardia|Congenital Heart Block
- Atrial Tachycardia
- Congenital Heart Block
- Atrial Fibrillation|Coronary artery disease
- Sporadic Alzheimer's disease
- Klinefelter syndrome
- Fragile X syndrome
- Fragile X premutation
- Charcot-Marie-Tooth disease type 2A
- Spinal Muscular Atrophy (Type II)
- Carrier of Spinal Muscular Atrophy (Type II)
- Spinal Muscular Atrophy (Type I)
- Amyotrophic lateral sclerosis
- Fragile X syndrome|Autism
- Rett syndrome
- Mental illness
- EIF3F gene mutation

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
- Male
- Female
- N/A

Genetic Alteration/Mutation
- CACNA1C
- KCTD13
- B2M
- HBB(E6V)
- HBB(E6V) Corrected
- HBB
- TPP1
- GFAP Corrected
- GFAP
- MYH11
- FMR1-FLAG
- FMR1 Knockout
- 47,XX,+21 (Trisomy 21)
- APPV717l mutation
- DYSF (heterozygous 1 mutation)
- DYSF (heterozygous 2 mutations)
- TAF1 variant (hemizygous carrier)
- TAF1 variant (homozygous carrier)
- TAF1 Variant (heterozygous carrier)
- TAF1 Variant
- TAF1 Variant Corrected
- PACS1
- PACS2
- LDLR(del exon3-6)homo
- ABC1(K531N)het
- ABCA1
- MTP(R46G)
- LDLR(del exon4-6)het
- ABC1(K531N)het; ABC1(S2046R)het
- SR-BI
- ABCA1(R1210stop)het; ABCA1(intron 32,G[-25]C)het
- BMPR2(R491W)
- ALK1
- APP (duplication)
- 47,XY,+21 (Trisomy 21)
- 47,XXY (Extra X chromosome)
- FMR1
- MFN2
- SMN1
- SOD1 > D90A
- SOD1 > D90A Corrected
- MECP2
- ADA
- CCR5
- DISC1 exon 8 wild-type mutation
- Whole exome sequencing revealed an autosomal recessive homozygous pathogenic variant in the EIF3F gene: c.694T>G/p.(Phe232Val)
- KCNQ1
- SCN5A

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

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

Provider
- 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
- 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, 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
- 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

Product Group
- Allen Institute-hESC
- BG-hESC
- Biotrophix-Pty
- Boston-Childrens-Hospital-Daley-PCBC
- Boston-Steinberg-iPSC
- Brigham-Womens-iPSC
- Brown-University
- Buck
- Choroideremia-Research-Foundation-Gamm
- ESI-hESC
- Framingham-Heart-Study
- Fred-Hutchinson-PCBC
- Jain-iPSC
- JHU-Becker-iPSC
- JHU-Zambidis-PCBC
- LT-hESC
- LT2-hESC
- Luebeck-Klein-iPSC
- Mass-General-iPSC
- Medical-College-of-Wisconsin-Broeckel
- PACS1-Syndrome
- PACS2
- Pennsylvania-Rader-iPSC
- Rockefeller-hESC
- SA-hESC
- Scripps-Topol-iPSC
- Stanford-Quertermous-iPSC
- Stanford-Rabinovitch-iPSC
- TE-hESC
- UCSD-Frazer-iPSC
- UCSD-Frazer-Restricted-iPSC
- UCSD-Goldstein-iPSC
- UCSD-Willert-hESC
- UCSF-hESC
- Univ-Washington-hESC
- University-Minnesota-Kyba-PCBC
- UW Slukvin-iPSC-(2)
- UW-Bhattacharyya-Down-Syndrome-iPSC
- UW-Bhattacharyya-Fragile-X-iPSC
- UW-Bhattacharyya-Fragile-X-iPSC-2
- UW-Bhattacharyya-Fragile-X-iPSC-3
- UW-Bhattacharyya-IIAM-iPSC
- UW-Chang-Rett-Syndrome-iPSC
- UW-Chang-Rett-Syndrome-iPSC-(3)
- UW-Slukvin
- UW-Slukvin-Modified-iPSC-(1)
- UW-Slukvin-Modified-WA01-Reporter
- UW-Svaren-Charcot-Marie-Tooth-iPSC
- UW-Terasawa-Modified-hESC
- UW-Zhang-Alexander
- UW-Zhang-ALS-iPSC
- UW-Zhang-DREADD
- UW-Zhang-Spinal-Muscular-Atrophy-iPSC
- WI-Clinical Grade
- WI-hESC
- WI-iPS

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

Reprogramming Method
- Viral Transfection (Retrovirus: Oct4, Klf4, Sox2, cMyc)
- Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, L-Myc, Nanog, Lin28, SV40LT)
- Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, cMyc)
- Viral transfection (Lentivirus: Oct4, Klf4, Sox2, cMyc)
- Non-integrating (Sendai: Oct3/4, Sox2, Klf4, cMyc)
- Viral transfection (Lentivirus: Oct4, Sox2, Nanog, Lin28)
- Non-integrating (OCT4, SOX2, NANOG, LIN28, L-MYC, KLF4, SV40LT)
- Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, cMyc, Bcl-xl)
- Non-integrating (Sendai: Oct4, Klf4, Sox2, cMyc)
- Non-Integrating (Episomal Plasmid: Oct3/4, shp53, Sox2, Klf4, LIN-28, L-myc)
- Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, LIN28A, I-Myc, TP53 knockdown)
- Non-Integrating (Episomal Plasmid: Oct4, Sox2, Klf4, LIN28, L-Myc, p53 shRNA)
- Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, L-Myc, shp53, Lin28)
- Sendai Virus (Oct4, Klf4, Sox2, Myc)
- Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, cMyc )
- Non-Integrating (Episomal plasmid: pEP4EO2SET2K (OCT4/SOX2/LT/KLF4), pEP4EO2SEN2K (OCT4/SOX2/NANOG/KLF4), and pCEP4-M2L (MYC/LIN28) plasmids)
- Transfection with a combination of pEP4EO2SET2K, pEP4EO2SEN2K and pCEP-M2L plasmids
- CRISPR/CAS9 technology using Addgene Plasmid ID 43861: mammalian codon optimized Cas9 nuclease (JDS246) Addgene Plasmid ID 43860: guide RNA (gRNA) expression vector
- Non-integrating_Sendai virus

Cell Line	Cell Line Alias	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Ethnicity	Genetically Related Cell Lines	dbGaP Data
WC023i-SMA-GM232	SMA-3	Human iPS	Spinal Muscular Atrophy (Type I)	2 copies of the SMN2 gene and is homozygous for deletion of exons 7 and 8 of the SMN1 gene	Male	7 Months	Caucasian	No	No
WC024i-FXS-Nluc1	FX-iPSC-Nluc1	Modified Human iPS	Fragile X syndrome		Male	8 Years		No	No
WC026i-5807-3		Human iPS	None reported		Female	Neonatal	Caucasian	No	No
WC027i-5807-5		Human iPS	None reported		Female	Neonatal	Caucasian	No	No
WC028i-5807-6		Human iPS	None reported		Female	Neonatal	Caucasian	No	No
WC029i-5907-1		Human iPS	None reported		Male	Neonatal	African American	No	No
WC030i-5907-2		Human iPS	None reported		Male	Neonatal	African American	No	No
WC031i-5907-6		Human iPS	None reported		Male	Neonatal	African American	No	No
WC032i-6007-1		Human iPS	None reported		Male	Neonatal	Asian	No	No
WC034i-SOD1-D90A		Human iPS	Amyotrophic lateral sclerosis		Female	50 Years	Caucasian	No	No

1…151152153…155

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