Cell Line Search

Showing 1169–1184 of 1589 results

Cell Line	Cell Line Alias	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Ethnicity	Genetically Related Cell Lines	dbGaP Data
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
WC024i-FXS-Nluc1	FX-iPSC-Nluc1	Modified Human iPS	Fragile X syndrome		Male	8 Years		No	No
WC026i-5807-3		Human iPS	None reported		Female	Neonatal	Caucasian	No	No
WC027i-5807-5		Human iPS	None reported		Female	Neonatal	Caucasian	No	No
WC028i-5807-6		Human iPS	None reported		Female	Neonatal	Caucasian	No	No
WC029i-5907-1		Human iPS	None reported		Male	Neonatal	African American	No	No

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