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 the Cell Line Inquiry Form.

Academic Pricing

Industry Pricing

$650 per cell line $950 per cell line

Further pricing information 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

Line
Parent Tissue
Associated Disease
Comments
Gender
Age
CS00iCTR-nxx Fibroblast None (Parent line GM05400) Clinically Normal Male 6
CS01iCNL-nxx Corneal Epithelial Cells Diabetes Clinically Normal Male Unknown
CS01iMEC-nxx Mammary Epithelial Cells Breast Cancer Clinically Normal Female Unknown
CS0003iCTR-nxx Peripheral Blood None Clinically Normal Male 34
CS0002iCTR-nxx Peripheral Blood None Clinically Normal Male 51
CS0007iCTR-nxx Peripheral Blood None Clinically Normal Male 60
CS03iCTR-nxx Fibroblast Monocarboxylate Transporter 8 (MCT8) Deficiency Clinically normal, father of CS01iMCT8-nxx Male Unknown
CS06iCTR-nxx Fibroblast Familial Alzheimer's Disease (FAD) (Parent line GM01706) Clinically normal Female 82
CS14iCTR-nxx Fibroblast Spinal Muscular Atrophy (SMA) (Parent line GM03814) 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 CS13iSMA1-nxx Female Unknown
CS14iCTR-21nxx Fibroblast Huntington's Disease (HD) Clinically Normal, Wife of affected patient, 21 CAG repeats Female 52
CS15iCTR-nxx Fibroblast Spinal Muscular Atrophy (SMA) (Parent line GM03815) Clinically normal; 2 affected children; father of CS13iSMA1-nxx Male Unknown
CS17iCTR-nx Activated Corneal Keratocytes Keratoconus (KC) Clinically Normal Female Unknown
CS21iCNL-nxx Corneal Epithelial Cells Diabetes Clinically Normal Male Unknown
CS26iCNL-nxx Corneal Epithelial Cells Diabetes Clinically Normal Female Unkonwn
CS25iCTR-18nxx Fibroblast Huntington's Disease (HD) Clinically Normal, brother of affected sibling, 18,17 CAG Repeats Male 76
CS38iCNL-nxx Corneal Epithelial Cells Diabetes Clinically Normal Male Unknown
CS68iASC-nxx Adipose Stem Cells Normal Clinically Normal Female Unknown
CS71iCTR-20nxx Fibroblast Huntington's Disease (HD) Clinically Normal, CAG repeats are 20 Female 61
CS83iCTR-33nxx Fibroblast Huntington's Disease (HD) Clinically Normal; At risk (50%) for Huntington's Disease, 33 CAG repeats Female 21
CS87iCTR-nxx Lymphoblastoid cell line Spinal Muscular Atrophy (SMA) (Parent line GM23687) Clinically normal; unaffected mother of CS86iSMA-nxx Female Unknown
CS88iCTR-nxx Fibroblast None (Parent line GM19688) Clinically normal; 3 sons clinically affected with GSD IX Male 57
CS688iCTR-nxx Lymphoblastoid cell line Spinal Muscular Atrophy (SMA) (Parent line GM23688) Clinically normal; unaffected father of CS86iSMA-nxx Male Unknown
CS888iCTR-nxx PBMC None Clinically normal Female 35


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Lothian Birth Cohort Control Lines

Line
Parent Tissue
Mutation/Comments
Gender
Age
CS0036iCTR-LBCnxx PBMC Clinically Normal Male 62
CS0459iCTR-LBCnxx PBMC Clinically Normal Female 78.67
CS0465iCTR-LBCnxx PBMC Clinically Normal Female 78.68
CS0594iCTR-LBCnxx PBMC Clinically Normal Female 79.22
CS0484iCTR-LBCnxx PBMC Clinically Normal Female 78.79
CS1050iCTR-LBCnxx PBMC Clinically Normal Male 80.26
CS0424iCTR-LBCnxx PBMC Clinically Normal Female 79.29
CS0702iCTR-LBCnxx PBMC Clinically Normal Male 79.1
CS0172iCTR-LBCnxx PBMC Clinically Normal Male 79.1
CS0791iCTR-LBCnxx PBMC Clinically Normal Female 79.1
CS1034iCTR-LBCnxx PBMC Clinically Normal Female 79.42
CS0908iCTR-LBCnxx PBMC Clinically Normal Male 79.67
CS0771iCTR-LBCnxx PBMC Clinically Normal Male 79.19
CS0228iCTR-LBCnxx PBMC Clinically Normal Female 78.98
CS1045iCTR-LBCnxx PBMC Clinically Normal Female 79.65
CS0617iCTR-LBCnxx PBMC Clinically Normal Male 79.22
CS1185iCTR-LBCnxx PBMC Clinically Normal Female 79.85
CS1031iCTR-LBCnxx PBMC Clinically Normal Female 80.13
CS0188iCTR-LBCnxx PBMC Clinically Normal Male 80.13
CS0395iCTR-LBCnxx PBMC Clinically Normal Male 78.8
CS0087iCTR-LBCnxx PBMC Clinically Normal Male 79.45


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Reporter Control Lines

Line
Parent Tissue
Mutation/Comments
Gender
Age
CS83iCTR-ACTB::nGFP-#46 Fibroblast Nuclear GFP in AAVS1 safe harbor locus, driven by ubiquitous beta-actin promoter. Female Unknown
UW-H9-ACTB::nLUC-#2 H9 hESCs Nuclear Luciferase in AAVS1 safe harbor locus, driven by ubiquitous beta-actin promoter. Female Unknown


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Amyotrophic Lateral Sclerosis (ALS)

Line
Parent Tissue
Mutation/Comments
Gender
Age
CS28iALS-C9nxx Fibroblast C9orf72 hexanucleotide repeat expansion (6-8kb expanded allele). Age of onset: 46; Site of onset: left upper extremity. Male 47
CS29iALS-C9nxx Fibroblast C9orf72 hexanucleotide repeat expansion (6-8kb expanded allele). Age of onset: 46; Site of onset: left lower extremity. Male 47
CS30iALS-C9nxx Fibroblast 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 51
CS52iALS-C9nxx Fibroblast C9orf72 hexanucleotide repeat expansion (6-8 kb). ALS, Age of onset: 57; mo disease duration, 48; Site of onset: Left upper extremity. Male 49
CS58iALS-C9NTnxx PBMC C9ORF72 Male 61
CS134iALS-C9Tnxx PBMC C9ORF72 Male 49
CS98iALS-Tnxx PBMC Sporadic Female 64
CS14isALS-Tnxx PBMC Sporadic Male 42
CS138isALS-Tnxx PBMC Sporadic Male 66
CS152isALS-Tnxx PBMC Sporadic Female 68
CS166isALS-Tnxx PBMC Sporadic Female 56
CS36isALS-nxx Lymphoblastoid cell line Sporadic Female 32
CS46isALS-nxx Lymphoblastoid cell line Sporadic Male 37
CS47iALS-TDPnxx Fibroblast Identified Mutation: GLY298SER; ALS 10, with out front temporal dementia with TDP43 inclusions; Age of Onset: 62 yr: Site of Symptom Onset: Limb-lower Male 64
CS37iALS-FUSnxx Fibroblast FUS Female 47
CS04iALS-SOD1H44Rnxx Fibroblast SOD1 Female 35
CS07iALS-SOD1A4Vnxx Fibroblast SOD1 Female 40
CS118iALS-SOD1l113Tnxx Fibroblast SOD1 Female 73
CS11iALS-SOD1l114Tnxx Fibroblast SOD1 Male 57
CS22iALS-SOD1l114Tnxx Fibroblast SOD1 Male 51
CS24iALS-SOD1E50Knxx Fibroblast SOD1 Female 49
CS367iALS-SOD1A89Vnxx Fibroblast SOD1 Male 45
CS53iALS-SOD1A4VNTnxx Fibroblast SOD1 Male 35


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ALS Isogenic Control Lines

Line
Parent Tissue
Mutation/Comments
Gender
Age
CS29iALS-C9n1.ISOxx Fibroblast Isogenic control line of CS29iALS-nxx Male Unknown
CS52iALS-C9n6.ISOxx Fibroblast Isogenic control line of CS52iALS-nxx Male Unknown


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Breast Cancer (BRCA1)

Line
Parent Tissue
Mutation/Comments
Gender
Age
CS08iBRCA-nxx Lymphoblastoid cell line Mutation in the breast cancer 1, early onset (BRCA1) gene. Female Unknown
CS70iBRCA-nxx Lymphoblastoid cell line Mutation in the breast cancer 1, early onset (BRCA 1) gene. Female Unknown
CS79iBRCA-nxx Lymphoblastoid cell line Mutation in the breast cancer 1, early onset (BRCA 1) gene. Female Unknown


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

Line
Parent Tissue
Mutation/Comment
Gender
Age
CS40iCMT-nxx Fibroblast Unknown Male Unknown
CS41iCMT-nxx Fibroblast Unknown Female Unknown
CS42iCMT-nxx Fibroblast Unknown Female Unknown
CS50iCMT-nxx Fibroblast Unknown Female Unknown
CS67iCMT-nxx Fibroblast Unknown Male Unknown
CS79iCMT-nxx Fibroblast Unknown Female Unknown


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Diabetes (DCNL)

Line
Parent Tissue
Mutation/Comment
Gender
Age
CS03iDCNL-nxx Corneal epithelial cells Type 1 Diabetes Female Unknown
CS04iDCNL-nxx Corneal epithelial cells Type 1 Diabetes Male Unknown
CS15iDCNL-nxx Corneal epithelial cells Type 1 Diabetes Male Unknown


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Familial Alzheimer's Disease (FAD)

Line
Parent Tissue
Mutation/
Comments
Gender
Age
CS08iFAD-nxx Fibroblast 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 81
CS40iFAD-nxx Fibroblast Alzheimer's Disease, Familial, Type 3; Cells carry missense mutation {Ala246Glu (A246E)} in the AD3 [presenilin 1 (PSEN1)] gene Male 56


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Huntington's Disease (HD)

Line
Parent Tissue
Mutation/
Comments
Gender
Age
CS25iCTR-18nxx Fibroblast Clinically Normal, brother of affected sibling, 18,17 CAG Repeats Male 76
CS71iCTR-20nxx Fibroblast Clinically Normal, CAG repeats are 20 Female Unknown
CS14iCTR-21nxx Fibroblast Clinically Normal, Wife of affected patient, 21 CAG repeats Female 52
CS83iCTR-33nxx Fibroblast Clinically Normal; At risk (50%) for Huntington's Disease, 33 CAG repeats (Parent line GM02183 from Coriell Cell Repositories) Female 21
CS13iHD-43nxx Fibroblast Clinically affected, 43 CAG Repeats Male 54
CS04iHD-46nxx Fibroblast Clinically affected, 46 CAG Repeats Female Unknown
CS87iHD-50nxx Fibroblast Clinically Affected; onset at age 27 yrs; neurological exam 3/82 shows mild chorea, marginal dystonia, hypomimia, and bradykinesia; 50 CAG repeats (Parent line GM04687 from Coriell Cell Repositories) Female 87
CS03iHD-53nxx Fibroblast Clinically affected, 53 CAG Repeats Male Unknown
CS92iHD-57nxx Fibroblast Clinically Affected, 57, 17 CAG repeats Female 29
CS21iHD-60nxx Fibroblast Onset at age 18 years; similarly affected grandmother and father; 46,XX. HTT 18 and 60. CAG repeats (Parent line GM03621 from Coriell Cell Repositories) Female 29
CS02iHD-66nxx Fibroblast Clinically affected, 66 CAG Repeats Male Unknown
CS81iHD-71nxx Fibroblast 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 71 (Parent line GM04281 from Coriell Cell Repositories) Female 20
CS77iHD-77nxx Fibroblast Clinically affected, 77 CAG Repeats Male Unknown
CS09iHD-109nxx Fibroblast Clinically Affected; 109, 19 CAG repeats Female Unknown
CS97iHD-180nxx Fibroblast Clinically Affected; 180 and 18 CAG repeats (Parent line GM09197 from Coriell Cell Repositories) Male 6


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Keratoconus (KC)

Line
Parent Tissue
Mutation/Comments
Gender
Age
CS67iKC-nxx Activated fibroblast from primary keratocytes Unknown Male Unknown
CS88iKC-nxx Activated fibroblast from primary keratocytes Unknown Female Unknown


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Monocarboxylate Transporter 8 (MCT8) Deficiency

Line
Parent Tissue
Mutation/Comment
Gender
Age
CS01iMCT8-nxx Fibroblast Mutation: P321L; Location of Mutation: TM5 Unknown Unknown
CS02iMCT8-nxx Fibroblast Unknown Female Unknown
CS06iMCT8-nxx Fibroblast Unknown Male Unknown
CS58iMCT8-nxx Fibroblast Mutation: A404fs416X; Location of Mutation: truncates TM7 Male Unknown


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Parkinson's Disease (PD)

Line
Parent Tissue
Mutation/Comments
Gender
Age
CS27iPD-nxx Lymphoblastoid cell line Young Onset Parkinson's Disease. REM Behavior Disorder Female 48
CS78iPD-nxx Lymphoblastoid cell line Caucasian male from USA Male 67


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Primary Lateral Sclerosis (PLS)

Line
Parent Tissue
Mutation/Comments
Gender
Age
CS51iPLS-nxx Lymphoblastoid cell line Unknown Male 55
CS89iPLS-nxx Lymphoblastoid cell line Unknown Male 62


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Obesity (OBS)

Line
Parent Tissue
Mutation/Comments
Gender
Age
CS02iOBS-nxx Lymphoblastoid cell line Body mass index = 50; 389 pounds; diabetes; enteritis; hypertension; hyperthyroidism; family history of diabetes and hyperthyroidism; obese spouse & son are GM14303 and GM14304, respectively (Parent line GM14302 from Coriell Cell Repository) Female 45
CS03iOBS-nxx Lymphoblastoid cell line Body mass index = 50; 400 pounds; diabetes; arthritis; hypertension; family history of diabetes, obesity, and hypertension; obese spouse and son are GM14302 and GM14304, respectively (Parent line GM14303 from Coriell Cell Repositories) Male 53
CS74iOBS-nxx Lymphoblastoid cell line Body mass index = 50; 319 pounds (Parent line GM14274 from Coriell Cell Repositories) Female 36
CS77iOBS-nxx Lymphoblastoid cell line Body mass index > 50; 400 pounds; bad hips; mother and grandmother are obese; mother is GM14278 (Parent line GM14277 from Coriell Cell Repositories)  Female 15
CS90iOBS-nxx Lymphoblastoid cell line Body mass index > 50; 330 pounds; irregular menses (Parent line GM14290 from Coriell Cell Repositories) Female 18


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Skeletal Dysplasia (SKD)

Line
Parent Tissue
Mutation/Comments
Gender
Age
CS01iSKD-nxx Fibroblast Metatropic dysplasia, Mild; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: E797K, C-Terminus; Autosomal Dominant Male Unknown
CS23iSKD-nxx Fibroblast Metatropic dysplasia, Lethal; Age of Onset: Neonatal (1st 30 days of life); TRPV4 Mutation: I604M, S4-S5 loop transmembrane; Autosomal Dominant Female Unknown
CS41iSKD-nxx Fibroblast Metatropic dysplasia, Lethal; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: K197R, Ankyrin 2; Autosomal Dominant Male Unknown
CS64iSKD-nxx Fibroblast Metatropic dysplasia, Moderate; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: P799L, C-Terminus; Autosomal Dominant Male Unknown
CS84iSKD-nxx Fibroblast Metatropic dysplasia, Moderate; Age of Onset: Infantile (1st year of life); TRPV4 Mutation: P799S, C-Terminus; Autosomal Dominant Male Unknown


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Spinal Muscular Atrophy (SMA)

Line
Parent Tissue
Mutation/Comment
Gender
Age
CS14iCTR-nxx Fibroblast 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 CS13iSMA1-nxx Female Unknown
CS15iCTR-nxx Fibroblast Clinically normal; 2 affected children; father of CS13iSMA1-nxx Male Unknown
CS87iCTR-nxx Lymphoblastiod cell line Clinically normal; unaffected mother of CS86iSMA-nxx Female Unknown
CS688iCTR-nxx Lymphoblastoid cell line Clinically normal; unaffected father of GM23686 Male Unknown
CS13iSMA-nxx Fibroblast Clinically affected; born after full term uncomplicated pregnancy; rolled over at 6 months old; began babbling at 9 months old; by 12 months old, there was marked muscle atrophy and weakness; absent deep tendon reflexes; constipation; donor subject has 3 copies of the SMN2 gene (data from several sources including Stabley et al. 2015, PMID 26247043); PCR analysis showed that this donor subject is homozygous for the deletion of exons 7 and 8 in the SMN1 gene; similarly affected brother (not in repository); mother is CS14iCTR-nxx) (Parent line GM03813 from Corielle Cell Repositories) Male 3
CS32iSMA-nxx Fibroblast 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. Progressive muscular atrophy; absent deep tendon reflexes; abnormal EMG; donor subject has 2 copies of the SMN2 gene (data from several sources including Stabley et al. 2015, PMID 26247043) and is homozygous for deletion of exons 7 and 8 of the SMN1 gene.  (Parent line GM00232 from Coriell Cell Repositories) Male 7 months
CS77iSMA1-nxx Fibroblast SMA Type I; Expired at age 23 months; negative family history;Expired at age 23 months; hypotonia; decreased muscle bulk; absent deep tendon reflexes; possible fasciculations; normal CPK; abnormal EMG and muscle biopsy consistent with the diagnosis; donor subject has 3 copies of the SMN2 gene (data from several sources including Stabley et al. 2015, PMID 26247043) and is homozygous for deletion of exons 7 and 8 of the SMN1 gene; negative family history; eye lens fibroblast culture. donor subject has 2 copies of the SMN2 gene and is homozygous for deletion of exons 7 and 8 of the SMN1 gene. (Parent line GM09677 from Coriell Cell Repositories) Male 2
CS83iSMA-nxx Fetal Fibroblast Unknown Male Fetal Sample
CS84iSMA1-nxx Lymphoblastoid cell line SMA Type I; donor subject is homozygous for deletion of exons 7 and 8 of the SMN1 gene and has 2 copies of the SExpired at age 6 months; marked diffuse hypotonia; respiratory distress; muscle atrophy; diagnosis confirmed by muscle biopsy; normal biotinidase level; donor subject is homozygous for a deletion of exons 7 and 8 in the SMN1 gene and has 2 copies of the SMN2 gene; negative family history. MN2 gene. Negative family history. (Parent line GM10684 from Coriell Cell Repositories) Female 6 months
CS86iSMA-nxx Lymphoblastoid cell line SMA Type I (Parent line GM23686 from Coriell Cell Repositories) Female Unknown
CS92iSMA2-nxx Fibroblast 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 (Parent line GM22592 from Coriell Cell Repositories) Male 1
CS55iSMA3-nxx Lymphoblastoid cell line SMA Type III, Clinically Affected (Parent line GM23255 from Coriell Cell Repositories) Male 16


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Spondylometaphyseal Dysplasias, Kozlowski type (SMDK)

Lines
Parent Tissue
Mutation/Comments
Gender
Age
CS44iSMDK-nxx Lymphoblastoid cell line Unknown Male Unknown
CS61iSMDK-nxx Lymphoblastoid cell line Unknown Female Unknown


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