Collection

Showing 49–64 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
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
WC053i-FX08-25	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
WC-24-02-DS-A		Human iPS	None reported		Female	25 Years	Caucasian	No	No
WC-24-02-DS-B		Human iPS	None reported		Female	25 Years	Caucasian	No	No
WC-24-02-DS-C		Human iPS	None reported		Female	25 Years	Caucasian	No	No

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