Stem Cell Lines

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-nxx

n1, n2, n18

Fibroblast

GM05400

Coriell Cell Repositories

None

Male

CS01iCNL-nxx

n1

Corneal Epithelial Cells

CNL01

Rabinowitz Lab

Diabetes

Male

CS01iMEC-nxx

n7, n8, n9

Mammary Epithelial Cells

hMEC 01

Cui Lab

Breast Cancer

Female

CS02iCTR-NTnxx

n1, n2, n3

Peripheral Blood

CS 002

Cedars-Sinai

None

Male

CS02iCTR-Tnxx

n10, n11, n22

Peripheral Blood

CS 002

Cedars-Sinai

None

Male

CS03iCTR-nxx

n1, n2, n3

Fibroblast

R4603

Sam Refetoff, University of Chicago

Monocarboxylate Transporter 8 (MCT8) Deficiency

Male

CS06iCTR-nxx

n1, n2

Fibroblast

GM01706

Coriell Cell Repositories

Familial Alzheimer's Disease (FAD)

Female

CS14iCTR-nxx

n5, n6, n8

Fibroblast

GM03814

Coriell Cell Repositories

Spinal Muscular Atrophy (SMA)

Female

CS14iCTR-21nxx

n2, n3

Fibroblast

ND30014

Coriell Cell Repositories

Huntington's Disease (HD)

Female

CS15iCTR-nxx

n5

Fibroblast

GM03815

Coriell Cell Repositories

Spinal Muscular Atrophy (SMA)

Male

CS17iCTR-nx

n1

Activated Corneal Keratocytes

AAM-417

Rabinowitz Lab

Keratoconus (KC)

Female

CS21iCNL-nxx

n1, n2, n11

Corneal Epithelial Cells

N13-21

Ljubimov Lab

Diabetes

Male

CS26iCNL-nxx

n1, n2, n3

Corneal Epithelial Cells

N13-26

Ljubimov Lab

Diabetes

Female

CS25iCTR-18nxx

n2, n5, n6

Fibroblast

ND30625

Coriell Cell Repositories

Huntington's Disease (HD)

Male

CS38iCNL-nxx

n1, n2, n3

Corneal Epithelial Cells

N13-38

Ljubimov Lab

Diabetes

Male

CS68iASC-nxx

n1, n3

Adipose Stem Cells

hASC68

Gazit Lab

Normal

Female

CS71iCTR-20nxx

n1, n3, n6

Fibroblast

ND29971

Coriell Cell Repositories

Huntington's Disease (HD)

Female

CS83iCTR-33nxx

n1, n2

Fibroblast

GM02183

Coriell Cell Repositories

Huntington's Disease (HD)

Female

CS87iCTR-nxx

n3, n12

EBV B-Cells

GM23687

Coriell Cell Repositories

Spinal Muscular Atrophy (SMA)

Female

CS88iCTR-nxx

n3, n5, n6

Fibroblast

GM19688

Coriell Cell Repositories

Familial Alzheimer's Disease (FAD)

Male

CS688iCTR-nxx

n2, n3, n5

EBV B-Cells

GM23688

Coriell Cell Repositories

Spinal Muscular Atrophy (SMA)

Male

Back to List

Reporter Control Lines

Line

Parent Tissue

Parent Line

Source

Description

Gender

CS83iCTR-ACTB::nGFP-#46

Fibroblast

GM02183

Coriell Cell Repositories

Nuclear GFP in AAVS1 safe harbor locus, driven by ubiquitous beta-actin promoter.

Female

UW-H9-ACTB::nLUC-#2

H9 hESCs

H9 hESCs

WiCell

Nuclear Luciferase in AAVS1 safe harbor locus, driven by ubiquitous beta-actin promoter.

Female

Back to List

Amyotrophic Lateral Sclerosis (ALS)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS28iALS-C9nxx

n1, n2

Fibroblast

F09128

Baloh Lab

C9orf72 hexanucleotide repeat expansion (6-8kb expanded allele). Age of onset: 46; Site of onset: left upper extremity.

Male

CS29iALS-C9nxx

n1

Fibroblast

F09229

Baloh Lab

C9orf72 hexanucleotide repeat expansion (6-8kb expanded allele). Age of onset: 46; Site of onset: left lower extremity.

Male

CS30iALS-C9nxx

n1

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

CS52iALS-C9nxx

n2, n4A, n4N

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

CS37iALS-FUSnxx

n1, n2, n3

Fibroblast

F10337

Baloh Lab

Currently Unavailable

Male

CS47iALS-TDPnxx

n1, n2, n5

Fibroblast

NA

Baloh Lab

Currently Unavailable

Male

Back to List

Breast Cancer (BRCA1)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS08iBRCA-nxx

n5, n8, n11

EBV B-Cells

2012-0376 4008

Cui Lab

Mutation in the breast cancer 1, early onset (BRCA1) gene.

Female

CS70iBRCA-nxx

n1, n2, n5

EBV B-Cells

4170

Cui Lab

Mutation in the breast cancer 1, early onset (BRCA1) gene.

Female

CS79iBRCA-nxx

n3, n9, n10

EBV B-Cells

2012-0872 4079

Cui Lab

Mutation in the breast cancer 1, early onset (BRCA1) gene.

Female

Back to List

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

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS41iCMT1A-nxx

n2, n4, n7

Fibroblast

F09141

Baloh Lab

Currently Unavailable.

Female

CS42iCMT1A-nxx

n2, n5, n6

Fibroblast

NA

Baloh Lab

Currently Unavailable

Female

CS50iCMT1A-nxx

n4, n5

Fibroblast

F09150

Baloh Lab

Currently Unavailable

Female

CS67iCMT1A-nxx

n1, n2, n4

Fibroblast

NA

Baloh Lab

Currently Unavailable

Female

Back to List

Diabetes (DCNL) 

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS03iDCNL-nxx

n2, n4

Diabetic Corneal Epithelial Cells

DM13-03

Ljubimov Lab

Type 1 Diabetes

Female

CS04iDCNL-nxx

n4

Diabetic Corneal Epithelial Cells

DM13-04

Ljubimov Lab

Type 1 Diabetes

Male

CS15iDCNL-nxx

n1, n2

Diabetic Corneal Epithelial Cells

DR13-15

Ljubimov Lab

Type 1 Diabetes

TBD

Back to List


Familial Alzheimer's Disease (FAD)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS06iCTR-nxx

n1, n2

Fibroblast

GM01706

Coriell Cell Repositories

Clinically normal

Female

CS88iCTR-nxx

n3, n5, n6

Fibroblast

GM19688

Coriell Cell Repositories

Clinically normal; 3 sons clinically affected with GSD IX

Male

CS08iFAD-nxx

n2, n4

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

CS40iFAD-nxx

n1, n2

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

Back to List

Huntington's Disease (HD)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS25iCTR-18nxx

n2, n5, n6

Fibroblast

ND30625

Coriell Cell Repositories

Clinically Normal, brother of affected sibling, CAG repeats are 18,17

Male

CS14iCTR-21nxx

n2, n3

Fibroblast

ND30014

Coriell Cell Repositories

Clinically Normal, Wife of affected patient, 21 CAG repeats

Female

CS71iCTR-20nxx

n1, n3, n6

Fibroblast

 

Coriell Cell Repositories

Clinically Normal, CAG repeats are 20

Female

CS83iCTR-33nxx

n1, n2

Fibroblast

GM02183

Coriell Cell Repositories

Clinically Normal; At risk (50%) for Huntington's Disease, 33 CAG repeats

Female

CS13iHD-43nxx

n2, n11, n13

Fibroblast

ND30013

Coriell Cell Repositories

Clinically Affected, CAG repeats are 43

Male

CS04iHD-46nxx

n1, n10

Fibroblast

HDF4 Q46

University of California, Irvine

Clinically Affected, CAG repeats are 46.

Male

CS87iHD-50nxx

n6, n7

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

CS03iHD-53nxx

n2, n3, n5

Fibroblast

HDF3

University of California, Irvine

Clinically Affected; CAG repeats are 53

Male

CS92iHD-57nxx

n2, n9

Fibroblast

ND33392

Coriell Cell Repositories

Clinically Affected, CAG repeats are 57, 17

Female

CS21iHD-60nxx

n5, n8

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

CS02iHD-66nxx

n4, n5, n8

Fibroblast

HDF2 Q66

University of California, Irvine

Clinically Affected, CAG repeats are 66

Female

CS81iHD-71nxx

n1, n3. n6

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

CS77iHD-77nxx

n3, n5, n9

Fibroblast

HD.77Q

Johns Hopkins University

Clinically Affected; CAG repeats are 77

Male

CS09iHD-109nxx

n1, n4, n5

Fibroblast

2024-7206 HD-109 Q

Johns Hopkins University

Clinically Affected; 109, 19 CAG repeats

Female

CS97iHD-180nxx

n1, n2, n3

Fibroblast

GM09197

Coriell Cell Repositories

Clinically Affected; 180 and 18 CAG repeats

Male

Back to List


Incontinentia Pigmenti (IP)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS93iIP-nxx

n1, n2, n6

Fibroblast

S11-30893T

Simmons Lab

Currently Unavailable

NA

Back to List

Keratoconus (KC) 

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS67iKC-nxx

n2, n4, n12

P-120-8367-OD

Activated fibroblast from primary keratocytes

Rabinowitz Lab

Unknown

Male

CS88iKC-nxx

n1, n5, n6

071-572-363/2911-531-2790

Activated fibroblast from primary keratocytes

Rabinowitz Lab

Unknown

Female

Back to List


Monocarboxylate Transporter 8 (MCT8) Deficiency

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS03iCTR-nxx

n1, n2, n3

Fibroblast

R4603

Sam Refetoff

Clinically Normal; Father of R4601

Male

CS01iMCT8-nxx

n2, n3, n5

Fibroblast

R4601

Sam Refetoff

Mutation: P321L; Location of Mutation: TM5

Male

CS58iMCT8-nxx

n1, n2, n4

Fibroblast

R2558

Sam Refetoff

Mutation: A404fs416X; Location of Mutation: truncates TM7

Male

Back to List

Neurofibromatosis Type 1 (NF1)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS22iNF1-nxx

n1

Fibroblast

GM00622

Coriell Cell Repositories

Clinically Affected

Male

Back to List


Skeletal Dysplasia (SKD)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS01iSKD-nxx

n2, n4, n5

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

CS23iSKD-nxx

n1, n12, n14

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

CS41iSKD-nxx

n1, n2, n5

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

CS64iSKD-nxx

n1, n2, n12

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

CS84iSKD-nxx

n1, n2, n5

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

Back to List

Spinal Muscular Atrophy (SMA)

Line

Clones

Parent Tissue

Parent Line

Source

Clinical History and Genetics

Gender

CS14iCTR-nxx

n5, n6, n8

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

CS15iCTR-nxx

n5

Fibroblast

GM03815

Coriell Cell Repositories

Clinically normal; 2 affected children; father of GM03813

Male

CS87iCTR-nxx

n3, n12

EBV B-Cells

GM23687

Coriell Cell Repositories

Clinically normal; unaffected mother of GM23686

Female

CS688iCTR-nxx

n2, n3, n5

EBV B-Cells

GM23688

Coriell Cell Repositories

Clinically normal; unaffected father of GM23686

Male

CS13iSMA1-nxx

n1

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

CS32iSMA1-nxx

n1, n3

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

CS77iSMA1-nxx

n5, n10

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

CS83iSMA-nxx

n2, n4, n5

EBV B-Cells

83 Fibroblast

Cedars-Sinai

Unknown

TBD

CS84iSMA1-nxx

n4C, n12B

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

CS92iSMA2-nxx

n1

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

CS55iSMA3-nxx

n1, n3

EBV B-Cells

GM23255

Coriell Cell Repositorie

SMA Type III, Clinically Affected

Male

Back to List

Android app on Google Play