Collection

Showing 1009–1024 of 1517 results

Cell Line	Cell Line Alias	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Ethnicity	Genetically Related Cell Lines	dbGaP Data
PENN170i-M17-4	iPS-M17-SeV4	Human iPS	Tangier disease	Zygosity compound heterozygous, Allele 1 p.R1210X, Allele 2 intron 32, -25 (G>C)	Male	43 Years	Asian	No	No
PENN171i-M9-9	M9-9	Human iPS	Homozygous Familial Hypercholesterolemia	Zygosity compound heterozygous, Allele1 p.W483X (old aa No: p. W462X), Allele 2 p.G549D (old aa No: p.G528D) http://www.ncbi.nlm.nih.gov/gene/3718	Male	22 Years	Caucasian	No	No
PENN172i-M15-10	M15-10	Human iPS	None reported		Female	62 Years	Caucasian	No	No
RUES1		Human ES	None reported		Male			No	No
RUES2		Human ES	None reported		Female			No	No
RUES3		Human ES	None reported		Male			No	No
SA01	SA001, Sahlgrenska 1	Human ES	None reported		Male			No	No
SA02	SA002, Sahlgrenska 2	Human ES	Patau Syndrome		Female			No	No
SCRP0104i	KBET0104i	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	59 Years	Caucasian > European	No	No
SCRP0202i	KBET0202i	Human iPS	Coronary artery disease\|Myocardial infarction	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	49 Years	Caucasian > European	No	No

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