Collection

Showing 1–16 of 1491 results

Cell Line	Cell Line Alias	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Ethnicity	Genetically Related Cell Lines	dbGaP Data
WC018i-CMT2A-3.3		Human iPS	None reported		Male			Yes	No
WC019i-SMA-GM13	SMA-1	Human iPS	Spinal Muscular Atrophy (Type II)	3 copies of SMN2 gene with homozygous deletion of exons 7 and 8 in SMN1 gene	Male	3 Years	Caucasian	Yes	No
WC020i-SMA-GM14	Contl-2	Human iPS	Carrier of Spinal Muscular Atrophy (Type II)	5 copies of SMN2 gene with heterozygous deletion of exons 7 and 8 in the SMN1 gene	Female		Caucasian	Yes	No
WC021i-SMA-GM15	Contl-3	Human iPS	Carrier of Spinal Muscular Atrophy (Type II)	1 copy of SMN2 gene	Male		Caucasian	Yes	No
WC022i-SMA-GM77	SMA-2	Human iPS	Spinal Muscular Atrophy (Type I)	3 copies of SMN2 gene with homozygous deletion of exons 7 and 8 in SMN1 gene	Male	2 Years	Caucasian	No	No
WC023i-SMA-GM232	SMA-3	Human iPS	Spinal Muscular Atrophy (Type I)	2 copies of the SMN2 gene and is homozygous for deletion of exons 7 and 8 of the SMN1 gene	Male	7 Months	Caucasian	No	No
WC034i-SOD1-D90A		Human iPS	Amyotrophic lateral sclerosis		Female	50 Years	Caucasian	No	No
WC035i-SOD1-D90D		Modified Human iPS	None reported		Female	50 Years	Caucasian	No	No
WC051i-FX08-23	FX08-1	Human iPS	Fragile X syndrome\|Autism	Full mutation FXS iPS cell line that lacks FMR1 and FMRP expression	Male	11 Years		No	No
WC052i-FX08-24	FX08-1	Human iPS	Fragile X syndrome\|Autism	Full mutation FXS iPS cell line that lacks FMR1 and FMRP expression	Male	11 Years		No	No