NHLBI Next Gen - Coronary artery disease and myocardial infarction (Dr. Eric Topol, Scripps Research Institute)

NHLBI Next Gen - Coronary artery disease and myocardial infarction (Dr. Eric Topol, Scripps Research Institute)

About Topol Lab’s Next Gen Cell Lines

This collection, from Dr. Eric Topol (Scripps), was generated to elucidate cardiovascular phenotypes employing genome editing of iPS cells.

The iPS cell lines in this collection were banked and characterized in the laboratories of Dr. Kristin Baldwin, Scripps Research Institute and Dr. Sheng Ding, Gladstone Institutes.

This collection contains 97 cell lines and includes genotyping of three sites within the 9p21 region for each donor. Disease states for the donors include coronary artery disease and myocardial infarction as well as individuals with no reported diagnosis. The age of donors range from 23-100 and ethnicities include Caucasian, European, and Latino.

About the Next Generation Genetic Association Studies (Next Gen) Program

These cell lines were created as Next Generation Genetic Association Studies (Next Gen) Program, which was a five-year, $80 million program to investigate functional genetic variation in humans by assessing cellular profiles that are surrogates for disease phenotypes. To achieve this, researchers from multiple institutions across the U.S. were awarded grants to derive iPS cell lines from more than 1,500 individuals representing various conditions as well as healthy controls for use in functional genomic (‘disease in a dish’) research. This extensive panel includes a diverse set of age, gender and ethnic backgrounds, and therefore will be an invaluable tool for evaluations across demographics. Further enhancing the utility of these cell lines are data sets such as phenotyping, GWAS, genome sequencing, gene expression and -omics analyses (e.g., lipidomic, proteomic, methylomic) that will be made available with the cell lines.

Showing 1–16 of 97 results

Showing 11 – 20 of 97 Cell Lines 97 Cell Lines Showing the single result No results found
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Cell Line
Cell Line Alias
Cell Type
Disease
Genetic Alteration/Mutation
Sex
Age at Collection
Ethnicity
Genetically Related Cell Lines
dbGaP Data
KBET0709i
Human iPS
Coronary artery disease
Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.
Male
79 Years
Caucasian
No
No
KBET0802i
Human iPS
None reported
Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.
Male
92 Years
Caucasian
No
No
HE01070
Human iPS
None reported
Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.
Female
85 Years
Caucasian > European
No
No
C00246
Human iPS
Coronary artery disease
Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.
Male
85 Years
Caucasian > European
No
No
HE01083
Human iPS
None reported
Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.
Male
91 Years
Caucasian
No
No
HE01187
Human iPS
None reported
Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.
Female
82 Years
Caucasian > European
No
No
HE01189
Human iPS
None reported
Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.
Female
87 Years
Caucasian
No
No
C00251
Human iPS
Coronary artery disease
Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the risk alleles at all 3 sites.
Male
90 Years
Caucasian > European
No
No
C00316
Human iPS
Coronary artery disease|Myocardial infarction
Three sites within the 9p21 region were genotyped for each donor. This donor was homozygous for the non-risk alleles at all 3 sites.
Female
76 Years
Caucasian
No
No
C00350
Human iPS
Coronary artery disease
Three sites within the 9p21 region were genotyped for each donor. This donor was heterozygous for the risk and non-risk alleles at all 3 sites.
Male
76 Years
Caucasian > European
No
No
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