Collection

Showing 1489–1491 of 1491 results

Cell Line	Cell Line Alias	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Genetically Related Cell Lines	dbGaP Data
WC007i-FX13-2	FX13-2	Human iPS	Fragile X syndrome		Male	8 Years	No	No
WC008i-C603-4	C603-4	Human iPS	None reported		Male	36 Years	No	No
WC010i-CMT2A-1.1		Human iPS	Charcot-Marie-Tooth disease type 2A	S249T mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene	Male		No	No
WC011i-CMT2A-1.2		Human iPS	Charcot-Marie-Tooth disease type 2A	S249T mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene	Male		No	No
WC012i-CMT2A-1.3		Human iPS	Charcot-Marie-Tooth disease type 2A	S249T mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene	Male		No	No
WC013i-CMT2A-2.1		Human iPS	Charcot-Marie-Tooth disease type 2A	H361y mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene	Male		Yes	No
WC014i-CMT2A-2.2		Human iPS	Charcot-Marie-Tooth disease type 2A	H361y mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene	Male		Yes	No
WC015i-CMT2A-2.3		Human iPS	Charcot-Marie-Tooth disease type 2A	H361y mutation resulting in a pathogenic variant of the Mitofusin 2 (MFN2) gene	Male		Yes	No
WC016i-CMT2A-3.1		Human iPS	None reported		Male		Yes	No
WC017i-CMT2A-3.2		Human iPS	None reported		Male		Yes	No

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