Stem Cell Lines

The iPSC lines generated by the Core are listed here, organized by disease and associated control(s). If you are interested in requesting any of these lines, please fill out out the Cell Line Inquiry Form. Prices for frozen vials and live cells can be found on our Services and Prices page

The table below will direct you to the disease or control of your interest. 

Control Lines

Diseased Lines

Control iPSC LinesAmyotrophic Lateral Sclerosis (ALS)   
Reporter Control iPSC LinesBreast Cancer (BRCA1)
 Charcot-Marie-Tooth Disease Type 1A (CMT1A)   
 Diabetes (DCNL)
 Familial Alzheimer's Disease (FAD)
 Huntington's Disease (HD)
 Incontinentia Pigmenti (IP)
 Keratoconus (KC)
 Monocarboxylate Transporter 8 (MCT8) Deficiency
 Neurofibromatosis Type 1 (NF1)
 Skeletal Dysplasia (SKD)
 Spinal Muscular Atrophy (SMA)

 

Control iPSC lines

Line

Clones

Parent Tissue

Parent Line

Source

Associated Disease

Gender

CS00iCTR-nxxn1, n2, n18FibroblastGM05400Coriell Cell RepositoriesNoneMale
CS01iCNL-nxxn1Corneal Epithelial CellsCNL01Rabinowitz LabDiabetesMale
CS01iMEC-nxxn7, n8, n9Mammary Epithelial CellshMEC 01Cui LabBreast CancerFemale
CS02iCTR-NTnxxn1, n2, n3Peripheral BloodCS 002Cedars-SinaiNoneMale
CS02iCTR-Tnxxn10, n11, n22Peripheral BloodCS 002Cedars-SinaiNoneMale
CS03iCTR-nxxn1, n2, n3FibroblastR4603Sam Refetoff, University of ChicagoMonocarboxylate Transporter 8 (MCT8) DeficiencyMale
CS06iCTR-nxxn1, n2FibroblastGM01706Coriell Cell RepositoriesFamilial Alzheimer's Disease (FAD)Female
CS14iCTR-nxxn5, n6, n8FibroblastGM03814Coriell Cell RepositoriesSpinal Muscular Atrophy (SMA)Female
CS14iCTR-21nxxn2, n3FibroblastND30014Coriell Cell RepositoriesHuntington's Disease (HD)Female
CS15iCTR-nxxn5FibroblastGM03815Coriell Cell RepositoriesSpinal Muscular Atrophy (SMA)Male
CS17iCTR-nxn1Activated Corneal KeratocytesAAM-417Rabinowitz LabKeratoconus (KC)Female
CS21iCNL-nxxn1, n2, n11Corneal Epithelial CellsN13-21Ljubimov LabDiabetesMale
CS26iCNL-nxxn1, n2, n3Corneal Epithelial CellsN13-26Ljubimov LabDiabetesFemale
CS25iCTR-18nxxn2, n5, n6FibroblastND30625Coriell Cell RepositoriesHuntington's Disease (HD)Male
CS38iCNL-nxxn1, n2, n3Corneal Epithelial CellsN13-38Ljubimov LabDiabetesMale
CS68iASC-nxxn1, n3Adipose Stem CellshASC68Gazit LabNormalFemale
CS71iCTR-20nxxn1, n3, n6FibroblastND29971Coriell Cell RepositoriesHuntington's Disease (HD)Female
CS83iCTR-33nxxn1, n2FibroblastGM02183Coriell Cell RepositoriesHuntington's Disease (HD)Female
CS87iCTR-nxxn3, n12EBV B-CellsGM23687Coriell Cell RepositoriesSpinal Muscular Atrophy (SMA)Female
CS88iCTR-nxxn3, n5, n6FibroblastGM19688Coriell Cell RepositoriesFamilial Alzheimer's Disease (FAD)Male
CS688iCTR-nxxn2, n3, n5EBV B-CellsGM23688Coriell Cell RepositoriesSpinal Muscular Atrophy (SMA)Male

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Reporter Control Lines

Line

Parent Tissue

Parent Line

Source

Description

Gender

CS83iCTR-ACTB::nGFP-#46FibroblastGM02183Coriell Cell RepositoriesNuclear GFP in AAVS1 safe harbor locus, driven by ubiquitous beta-actin promoter.Female
UW-H9-ACTB::nLUC-#2H9 hESCsH9 hESCsWiCellNuclear Luciferase in AAVS1 safe harbor locus, driven by ubiquitous beta-actin promoter.Female

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Amyotrophic Lateral Sclerosis (ALS)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS28iALS-C9nxxn1, n2FibroblastF09128Baloh LabC9orf72 hexanucleotide repeat expansion (6-8kb expanded allele). Age of onset: 46; Site of onset: left upper extremity.Male
CS29iALS-C9nxxn1FibroblastF09229Baloh LabC9orf72 hexanucleotide repeat expansion (6-8kb expanded allele). Age of onset: 46; Site of onset: left lower extremity.Male
CS30iALS-C9nxxn1FibroblastF10-330Baloh LabC9orf72 hexanucleotide repeat expansion (2.7 kb expanded allele). Age of onset: 51; 29 mo disease duration, Site of onset: Bulbar, Mildly decreased verbal fluency.Female
CS52iALS-C9nxxn2, n4A, n4NFibroblastF09152Baloh LabC9orf72 hexanucleotide repeat expansion (6-8 kb). ALS, Age of onset: 57; mo disease duration, 48; Site of onset: Left upper extremity.Male
CS37iALS-FUSnxxn1, n2, n3FibroblastF10337Baloh LabCurrently UnavailableMale
CS47iALS-TDPnxxn1, n2, n5FibroblastNACoriell Cell RepositoriesCurrently UnavailableMale

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Breast Cancer (BRCA1)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS08iBRCA-nxxn5, n8, n11EBV B-Cells2012-0376 4008Cui LabMutation in the breast cancer 1, early onset (BRCA1) gene.Female
CS70iBRCA-nxxn1, n2, n5EBV B-Cells4170Cui LabMutation in the breast cancer 1, early onset (BRCA1) gene.Female
CS79iBRCA-nxxn3, n9, n10EBV B-Cells2012-0872 4079Cui LabMutation in the breast cancer 1, early onset (BRCA1) gene.Female

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Charcot-Marie-Tooth Disease Type 1A (CMT1A)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS41iCMT1A-nxxn2, n4, n7FibroblastF09141Baloh LabCurrently Unavailable.Female
CS42iCMT1A-nxxn2, n5, n6FibroblastNABaloh LabCurrently UnavailableFemale
CS50iCMT1A-nxxn4, n5FibroblastF09150Baloh LabCurrently UnavailableFemale
CS67iCMT1A-nxxn1, n2, n4FibroblastNABaloh LabCurrently UnavailableFemale

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Diabetes (DCNL) 

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS03iDCNL-nxxn2, n4Diabetic Corneal Epithelial CellsDM13-03Ljubimov LabType 1 DiabetesFemale
CS04iDCNL-nxxn4Diabetic Corneal Epithelial CellsDM13-04Ljubimov LabType 1 DiabetesMale
CS15iDCNL-nxxn1, n2Diabetic Corneal Epithelial CellsDR13-15Ljubimov Lab

Type 1 Diabetes

TBD

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Familial Alzheimer's Disease (FAD)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS06iCTR-nxxn1, n2FibroblastGM01706Coriell Cell RepositoriesClinically normalFemale
CS88iCTR-nxxn3, n5, n6FibroblastGM19688Coriell Cell RepositoriesClinically normal; 3 sons clinically affected with GSD IXMale
CS08iFAD-nxxn2, n4FibroblastAG09908Coriell Cell Repositories

Alzheimer's Disease, Familial, Type 4; A heterozygous substitution (A>T at nucleotide 787) in the AD4 [presenilin 2 (PSEN2)] gene results in an Asn141Ile (N141I) missense mutation.

Female
CS40iFAD-nxxn1, n2FibroblastAG06840Coriell Cell RepositoriesAlzheimer's Disease, Familial, Type 3; Cells carry missense mutation {Ala246Glu (A246E)} in the AD3 [presenilin 1 (PSEN1)] geneMale

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Huntington's Disease (HD)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS25iCTR-18nxxn2, n5, n6FibroblastND30625Coriell Cell RepositoriesClinically Normal, brother of affected sibling, CAG repeats are 18,17Male
CS14iCTR-21nxxn2, n3FibroblastND30014Coriell Cell RepositoriesClinically Normal, Wife of affected patient, 21 CAG repeatsFemale
CS71iCTR-20nxxn1, n3, n6Fibroblast Coriell Cell RepositoriesClinically Normal, CAG repeats are 20Female
CS83iCTR-33nxxn1, n2FibroblastGM02183Coriell Cell RepositoriesClinically Normal; At risk (50%) for Huntington's Disease, 33 CAG repeatsFemale
CS13iHD-43nxxn2, n11, n13FibroblastND30013Coriell Cell RepositoriesClinically Affected, CAG repeats are 43Male
CS04iHD-46nxxn1, n10FibroblastHDF4 Q46University of California, IrvineClinically Affected, CAG repeats are 46.Male
CS87iHD-50nxxn6, n7FibroblastGM04687Coriell Cell RepositoriesClinically Affected; onset at age 27 yrs; neurological exam 3/82 shows mild chorea, marginal dystonia, hypomimia, and bradykinesia; CAG repeats are 50Female
CS03iHD-53nxxn2, n3, n5FibroblastHDF3University of California, IrvineClinically Affected; CAG repeats are 53Male
CS92iHD-57nxxn2, n9FibroblastND33392Coriell Cell RepositoriesClinically Affected, CAG repeats are 57, 17Female
CS21iHD-60nxxn5, n8FibroblastGM03621Coriell Cell RepositoriesOnset at age 18 years; similarly affected grandmother and father; 46,XX. HTT CAG repeats are 18 and 60.Female
CS02iHD-66nxxn4, n5, n8FibroblastHDF2 Q66University of California, IrvineClinically Affected, CAG repeats are 66Female
CS81iHD-71nxxn1, n3. n6FibroblastGM04281Coriell Cell RepositoriesRigid form of HD, possible homozygote, onset at age 14 yrs; neurological exam 3/82 shows a hypokinetic variant of HD with dystonia and marked tremor, ataxic wide-based gait; CAG repeats are 78Female
CS77iHD-77nxxn3, n5, n9FibroblastHD.77QJohns Hopkins UniversityClinically Affected; CAG repeats are 77Male
CS09iHD-109nxxn1, n4, n5Fibroblast2024-7206 HD-109 QJohns Hopkins UniversityClinically Affected; 109, 19 CAG repeatsFemale
CS97iHD-180nxxn1, n2, n3FibroblastGM09197Coriell Cell RepositoriesClinically Affected; 180 and 18 CAG repeatsMale

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Incontinentia Pigmenti (IP)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS93iIP-nxxn1, n2, n6FibroblastS11-30893TSimmons LabCurrently UnavailableNA

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Keratoconus (KC) 

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS67iKC-nxxn2, n4, n12P-120-8367-ODActivated fibroblast from primary keratocytesRabinowitz LabUnknownMale
CS88iKC-nxxn1, n5, n6071-572-363/2911-531-2790Activated fibroblast from primary keratocytesRabinowitz LabUnknownFemale

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Monocarboxylate Transporter 8 (MCT8) Deficiency

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS03iCTR-nxxn1, n2, n3FibroblastR4603Sam RefetoffClinically Normal; Father of R4601Male
CS01iMCT8-nxxn2, n3, n5FibroblastR4601Sam RefetoffMutation: P321L; Location of Mutation: TM5Male
CS58iMCT8-nxxn1, n2, n4FibroblastR2558Sam RefetoffMutation: A404fs416X; Location of Mutation: truncates TM7Male

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Neurofibromatosis Type 1 (NF1)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS22iNF1-nxxn1FibroblastGM00622Coriell Cell RepositoriesClinically AffectedMale

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Skeletal Dysplasia (SKD)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS01iSKD-nxxn2, n4, n5FibroblastR01-187International Skeletal Dysplasia RegistryMetatropic dysplasia, Mild; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: E797K, C-Terminus; Autosomal DominantMale
CS23iSKD-nxxn1, n12, n14FibroblastR08-023International Skeletal Dysplasia RegistryMetatropic dysplasia, Lethal; Age of Onset: Neonatal (1st 30 days of life); TRPV4 Mutation: I604M, S4-S5 loop transmembrane; Autosomal DominantFemale
CS41iSKD-nxxn1, n2, n5FibroblastR99-441 AInternational Skeletal Dysplasia RegistryMetatropic dysplasia, Lethal; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: K197R, Ankyrin 2; Autosomal DominantMale
CS64iSKD-nxxn1, n2, n12FibroblastR82-064International Skeletal Dysplasia RegistryMetatropic dysplasia, Moderate; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: P799L, C-Terminus; Autosomal DominantMale
CS84iSKD-nxxn1, n2, n5FibroblastR84-187International Skeletal Dysplasia RegistryMetatropic dysplasia, Moderate; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: P799S, C-Terminus; Autosomal DominantMale

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Spinal Muscular Atrophy (SMA)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS14iCTR-nxxn5, n6, n8FibroblastGM03814Coriell Cell RepositoriesClinically normal; 2 affected children; donor subject has two copies of the SMN2 gene; donor is heterozygous for deletion of exons 7 and 8 in the SMN1 gene; Mother of GM03813Female
CS15iCTR-nxxn5FibroblastGM03815Coriell Cell RepositoriesClinically normal; 2 affected children; father of GM03813Male
CS87iCTR-nxxn3, n12EBV B-CellsGM23687Coriell Cell RepositoriesClinically normal; unaffected mother of GM23686Female
CS688iCTR-nxxn2, n3, n5EBV B-CellsGM23688Coriell Cell RepositoriesClinically normal; unaffected father of GM23686Male
CS13iSMA1-nxxn1FibroblastGM03813Coriell Cell RepositoriesSMA Type I; donor subject has 2 copies of the SMN2 gene; donor subject is homozygous for the deletion of exons 7 and 8 in the SMN1 geneMale
CS32iSMA1-nxxn1, n3FibroblastGM00232Coriell Cell RepositoriesSMA Type I; donor subject has only one copy of the SMN2 gene and is homozygous for deletion of exons 7 and 8 of the SMN1 gene.Female
CS77iSMA1-nxxn5, n10FibroblastGM09677Coriell Cell RepositoriesSMA Type I; Expired at age 23 months; negative family history; donor subject has 2 copies of the SMN2 gene and is homozygous for deletion of exons 7 and 8 of the SMN1 gene.Male
CS83iSMA-nxxn2, n4, n5EBV B-Cells83 FibroblastCedars-SinaiUnknownTBD
CS84iSMA1-nxxn4C, n12BEBV B-CellsGM10684Coriell Cell RepositoriesSMA Type I; donor subject is homozygous for deletion of exons 7 and 8 of the SMN1 gene and has 2 copies of the SMN2 gene. Negative family history.Female
CS92iSMA2-nxxn1FibroblastGM22592Coriell Cell RepositoriesSMA Type II; donor subject is homozygous for deletion of exons 7 and 8 of the SMN1 gene and has 3 copies of the SMN2 geneMale
CS55iSMA3-nxxn1, n3EBV B-CellsGM23255Coriell Cell RepositorieSMA Type III, Clinically AffectedMale

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