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 Lines Amyotrophic Lateral Sclerosis (ALS)   
Reporter Control iPSC Lines Breast 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

Parent Tissue

Parent Line

Source

Associated Disease

Gender

Availability Status

CS00iCTR-nxx Fibroblast GM05400 Coriell Cell Repositories None Male Available
CS01iCNL-nxx Corneal Epithelial Cells CNL01 Rabinowitz Lab Diabetes Male Available
CS01iMEC-nxx Mammary Epithelial Cells hMEC 01 Cui Lab Breast Cancer Female Available
CS02iCTR-NTnxx Peripheral Blood CS 002 Cedars-Sinai None Male Available for Collaboration
CS02iCTR-Tnxx Peripheral Blood CS 002 Cedars-Sinai None Male Available for Collaboration
CS03iCTR-nxx Fibroblast R4603 Sam Refetoff, University of Chicago Monocarboxylate Transporter 8 (MCT8) Deficiency Male Available
CS06iCTR-nxx Fibroblast GM01706 Coriell Cell Repositories Familial Alzheimer's Disease (FAD) Female Available
CS14iCTR-nxx Fibroblast GM03814 Coriell Cell Repositories Spinal Muscular Atrophy (SMA) Female Available
CS14iCTR-21nxx Fibroblast ND30014 Coriell Cell Repositories Huntington's Disease (HD) Female Available
CS15iCTR-nxx Fibroblast GM03815 Coriell Cell Repositories Spinal Muscular Atrophy (SMA) Male Available
CS17iCTR-nx Activated Corneal Keratocytes AAM-417 Rabinowitz Lab Keratoconus (KC) Female Available
CS21iCNL-nxx Corneal Epithelial Cells N13-21 Ljubimov Lab Diabetes Male Available
CS26iCNL-nxx Corneal Epithelial Cells N13-26 Ljubimov Lab Diabetes Female Available
CS25iCTR-18nxx Fibroblast ND30625 Coriell Cell Repositories Huntington's Disease (HD) Male Available
CS38iCNL-nxx Corneal Epithelial Cells N13-38 Ljubimov Lab Diabetes Male Available
CS68iASC-nxx Adipose Stem Cells hASC68 Gazit Lab Normal Female Available
CS71iCTR-20nxx Fibroblast ND29971 Coriell Cell Repositories Huntington's Disease (HD) Female Available
CS83iCTR-33nxx Fibroblast GM02183 Coriell Cell Repositories Huntington's Disease (HD) Female Available
CS87iCTR-nxx EBV B-Cells GM23687 Coriell Cell Repositories Spinal Muscular Atrophy (SMA) Female Available
CS88iCTR-nxx Fibroblast GM19688 Coriell Cell Repositories Familial Alzheimer's Disease (FAD) Male Available
CS688iCTR-nxx EBV B-Cells GM23688 Coriell Cell Repositories Spinal Muscular Atrophy (SMA) Male Available

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Reporter Control Lines


Line

Parent Tissue

Parent Line

Source

Description

Gender

Availability Status

CS83iCTR-ACTB::nGFP-#46 Fibroblast GM02183 Coriell Cell Repositories Nuclear GFP in AAVS1 safe harbor locus, driven by ubiquitous beta-actin promoter. Female Available
UW-H9-ACTB::nLUC-#2 H9 hESCs H9 hESCs WiCell Nuclear Luciferase in AAVS1 safe harbor locus, driven by ubiquitous beta-actin promoter. Female Not Available

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Amyotrophic Lateral Sclerosis (ALS)


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS28iALS-C9nxx Fibroblast F09128 Baloh Lab C9orf72 hexanucleotide repeat expansion (6-8kb expanded allele). Age of onset: 46; Site of onset: left upper extremity. Male Available
CS29iALS-C9nxx Fibroblast F09229 Baloh Lab C9orf72 hexanucleotide repeat expansion (6-8kb expanded allele). Age of onset: 46; Site of onset: left lower extremity. Male Available
CS30iALS-C9nxx Fibroblast F10-330 Baloh Lab C9orf72 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 Available
CS52iALS-C9nxx Fibroblast F09152 Baloh Lab C9orf72 hexanucleotide repeat expansion (6-8 kb). ALS, Age of onset: 57; mo disease duration, 48; Site of onset: Left upper extremity. Male Available
CS37iALS-FUSnxx Fibroblast F10337 Baloh Lab Currently Unavailable Male Available
CS47iALS-TDPnxx Fibroblast ND32947 Coriell Cell Repositories Identified Mutation: GLY298SER; ALS 10, with out frontotemporal dementia with TDP43 inclusions; Age of Onset: 62 yr: Site of Symptom Onset: Limb-lower Male Available

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Breast Cancer (BRCA1)


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS08iBRCA-nxx EBV B-Cells 2012-0376 4008 Cui Lab Mutation in the breast cancer 1, early onset (BRCA1) gene. Female Available for Collaboration
CS70iBRCA-nxx EBV B-Cells 4170 Cui Lab Mutation in the breast cancer 1, early onset (BRCA1) gene. Female Available for Collaboration
CS79iBRCA-nxx EBV B-Cells 2012-0872 4079 Cui Lab Mutation in the breast cancer 1, early onset (BRCA1) gene. Female Available for Collaboration

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


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS41iCMT1A-nxx Fibroblast F09141 Baloh Lab Currently Unavailable. Female Available
CS42iCMT1A-nxx Fibroblast NA Baloh Lab Currently Unavailable Female Available
CS50iCMT1A-nxx Fibroblast F09150 Baloh Lab Currently Unavailable Female Available
CS67iCMT1A-nxx Fibroblast NA Baloh Lab Currently Unavailable Female Available

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Diabetes (DCNL) 


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS03iDCNL-nxx Diabetic Corneal Epithelial Cells DM13-03 Ljubimov Lab Type 1 Diabetes Female Available
CS04iDCNL-nxx Diabetic Corneal Epithelial Cells DM13-04 Ljubimov Lab Type 1 Diabetes Male Available
CS15iDCNL-nxx Diabetic Corneal Epithelial Cells DR13-15 Ljubimov Lab

Type 1 Diabetes

Male Available

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Familial Alzheimer's Disease (FAD)


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS06iCTR-nxx Fibroblast GM01706 Coriell Cell Repositories Clinically normal Female Available
CS88iCTR-nxx Fibroblast GM19688 Coriell Cell Repositories Clinically normal; 3 sons clinically affected with GSD IX Male Available
CS08iFAD-nxx Fibroblast AG09908 Coriell 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 Available
CS40iFAD-nxx Fibroblast AG06840 Coriell Cell Repositories Alzheimer's Disease, Familial, Type 3; Cells carry missense mutation {Ala246Glu (A246E)} in the AD3 [presenilin 1 (PSEN1)] gene Male Available

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Huntington's Disease (HD)


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS25iCTR-18nxx Fibroblast ND30625 Coriell Cell Repositories Clinically Normal, brother of affected sibling, CAG repeats are 18,17 Male Available
CS14iCTR-21nxx Fibroblast ND30014 Coriell Cell Repositories Clinically Normal, Wife of affected patient, 21 CAG repeats Female Available
CS71iCTR-20nxx Fibroblast  ND29971 Coriell Cell Repositories Clinically Normal, CAG repeats are 20 Female Available
CS83iCTR-33nxx Fibroblast GM02183 Coriell Cell Repositories Clinically Normal; At risk (50%) for Huntington's Disease, 33 CAG repeats Female Available
CS13iHD-43nxx Fibroblast ND30013 Coriell Cell Repositories Clinically Affected, CAG repeats are 43 Male Available
CS04iHD-46nxx Fibroblast HDF4 Q46 University of California, Irvine Clinically Affected, CAG repeats are 46. Male Available
CS87iHD-50nxx Fibroblast GM04687 Coriell Cell Repositories Clinically Affected; onset at age 27 yrs; neurological exam 3/82 shows mild chorea, marginal dystonia, hypomimia, and bradykinesia; CAG repeats are 50 Female Available
CS03iHD-53nxx Fibroblast HDF3 University of California, Irvine Clinically Affected; CAG repeats are 53 Male Available
CS92iHD-57nxx Fibroblast ND33392 Coriell Cell Repositories Clinically Affected, CAG repeats are 57, 17 Female Available
CS21iHD-60nxx Fibroblast GM03621 Coriell Cell Repositories Onset at age 18 years; similarly affected grandmother and father; 46,XX. HTT CAG repeats are 18 and 60. Female Available
CS02iHD-66nxx Fibroblast HDF2 Q66 University of California, Irvine Clinically Affected, CAG repeats are 66 Female Available
CS81iHD-71nxx Fibroblast GM04281 Coriell Cell Repositories Rigid 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 78 Female Available
CS77iHD-77nxx Fibroblast HD.77Q Johns Hopkins University Clinically Affected; CAG repeats are 77 Male Available
CS09iHD-109nxx Fibroblast 2024-7206 HD-109 Q Johns Hopkins University Clinically Affected; 109, 19 CAG repeats Female Available
CS97iHD-180nxx Fibroblast GM09197 Coriell Cell Repositories Clinically Affected; 180 and 18 CAG repeats Male Available

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Incontinentia Pigmenti (IP)


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS93iIP-nxx Fibroblast S11-30893T Simmons Lab Currently Unavailable NA Not Available

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Keratoconus (KC) 


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS67iKC-nxx P-120-8367-OD Activated fibroblast from primary keratocytes Rabinowitz Lab Unknown Male Available
CS88iKC-nxx 071-572-363/2911-531-2790 Activated fibroblast from primary keratocytes Rabinowitz Lab Unknown Female Available

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Monocarboxylate Transporter 8 (MCT8) Deficiency


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS03iCTR-nxx Fibroblast R4603 Sam Refetoff Clinically Normal; Father of R4601 Male Available
CS01iMCT8-nxx Fibroblast R4601 Sam Refetoff Mutation: P321L; Location of Mutation: TM5 Male Available
CS58iMCT8-nxx Fibroblast R2558 Sam Refetoff Mutation: A404fs416X; Location of Mutation: truncates TM7 Male Available

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Neurofibromatosis Type 1 (NF1)


Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS22iNF1-nxx n1 Fibroblast GM00622 Coriell Cell Repositories Clinically Affected Male Not Available

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Skeletal Dysplasia (SKD)


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS01iSKD-nxx Fibroblast R01-187 International Skeletal Dysplasia Registry Metatropic dysplasia, Mild; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: E797K, C-Terminus; Autosomal Dominant Male Available
CS23iSKD-nxx Fibroblast R08-023 International Skeletal Dysplasia Registry Metatropic dysplasia, Lethal; Age of Onset: Neonatal (1st 30 days of life); TRPV4 Mutation: I604M, S4-S5 loop transmembrane; Autosomal Dominant Female Available
CS41iSKD-nxx Fibroblast R99-441 A International Skeletal Dysplasia Registry Metatropic dysplasia, Lethal; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: K197R, Ankyrin 2; Autosomal Dominant Male Available
CS64iSKD-nxx Fibroblast R82-064 International Skeletal Dysplasia Registry Metatropic dysplasia, Moderate; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: P799L, C-Terminus; Autosomal Dominant Male Available
CS84iSKD-nxx Fibroblast R84-187 International Skeletal Dysplasia Registry Metatropic dysplasia, Moderate; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: P799S, C-Terminus; Autosomal Dominant Male Available

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Spinal Muscular Atrophy (SMA)


Line

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

Availability Status

CS14iCTR-nxx Fibroblast GM03814 Coriell Cell Repositories Clinically 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 GM03813 Female Available
CS15iCTR-nxx Fibroblast GM03815 Coriell Cell Repositories Clinically normal; 2 affected children; father of GM03813 Male Available
CS87iCTR-nxx EBV B-Cells GM23687 Coriell Cell Repositories Clinically normal; unaffected mother of GM23686 Female Available
CS688iCTR-nxx EBV B-Cells GM23688 Coriell Cell Repositories Clinically normal; unaffected father of GM23686 Male Available
CS13iSMA1-nxx Fibroblast GM03813 Coriell Cell Repositories SMA 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 gene Male Available
CS32iSMA1-nxx Fibroblast GM00232 Coriell Cell Repositories SMA 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 Available
CS77iSMA1-nxx Fibroblast GM09677 Coriell Cell Repositories SMA 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 Available
CS83iSMA-nxx Fetal Fibroblast 83 Fibroblast Cedars-Sinai Unknown Male Available
CS84iSMA1-nxx EBV B-Cells GM10684 Coriell Cell Repositories SMA 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 Available
CS92iSMA2-nxx Fibroblast GM22592 Coriell Cell Repositories SMA Type II; donor subject is homozygous for deletion of exons 7 and 8 of the SMN1 gene and has 3 copies of the SMN2 gene Male Available
CS55iSMA3-nxx EBV B-Cells GM23255 Coriell Cell Repositorie SMA Type III, Clinically Affected Male Available

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