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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
- 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

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

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)
- ETV2
- FMR1
- MFN2
- SMN1
- SOD1 > D90A
- SOD1 > D90A Corrected
- MECP2
- ADA
- CCR5
- DISC1 exon 8 wild-type mutation
- 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
  - Vascular
  - Vascular - Smooth Muscle Cells
  - Endothelial|Reporter; Hematopoetic
  - Constitutive
  - Cardiac
  - Endothelial
- 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
- 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

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)
- Skin Fibroblast (GM07982)
- Blood (GM20920)
- Blood (GM01715)
- Lung Fibroblast

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

Cell Line	Cell Line Alias	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Ethnicity	Genetically Related Cell Lines	dbGaP Data
PENN168i-M16-1	M16-SeV1	Human iPS	Homozygous Familial Hypercholesterolemia	Zygosity compound heterozygous, Allele 1 p.E605E fs 38X, Allele 2 del exons 4-6 http://www.ncbi.nlm.nih.gov/gene/3718	Female	28 Years	Latino\|Native American	No	No
PENN169i-M17-3	iPS-M17-SeV3	Human iPS	Tangier disease	Zygosity compound heterozygous, Allele 1 p.R1210X, Allele 2 intron 32, -25 (G>C)	Male	43 Years	Asian	No	No
PENN170i-M17-4	iPS-M17-SeV4	Human iPS	Tangier disease	Zygosity compound heterozygous, Allele 1 p.R1210X, Allele 2 intron 32, -25 (G>C)	Male	43 Years	Asian	No	No
PENN171i-M9-9	M9-9	Human iPS	Homozygous Familial Hypercholesterolemia	Zygosity compound heterozygous, Allele1 p.W483X (old aa No: p. W462X), Allele 2 p.G549D (old aa No: p.G528D) http://www.ncbi.nlm.nih.gov/gene/3718	Male	22 Years	Caucasian	No	No
PENN172i-M15-10	M15-10	Human iPS	None reported		Female	62 Years	Caucasian	No	No
RUES1		Human ES	None reported		Male			No	No
RUES2		Human ES	None reported		Female			No	No
RUES3		Human ES	None reported		Male			No	No
SA01	SA001, Sahlgrenska 1	Human ES	None reported		Male			No	No
SA02	SA002, Sahlgrenska 2	Human ES	Patau Syndrome		Female			No	No

1…787980…155

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