Cell Line Search

Showing 1457–1472 of 1589 results

Cell Line	Cell Type	Disease	Genetic Alteration/Mutation	Sex	Age at Collection	Ethnicity	Genetically Related Cell Lines	dbGaP Data
Zeng01i-iPSH9	Human iPS	None reported		Female			No	No
Zeng02i-iPSH14	Human iPS	None reported		Male			No	No
EIFIIIi001-A	Human iPS	EIF3F-associated Neurodevelopmental Disorder	Whole exome sequencing revealed an autosomal recessive homozygous pathogenic variant in the EIF3F gene: c.694T>G/p.(Phe232Val)	Female	6 years	Caucasian > European	No	No
UCSD242i-LQT1-1	Modified Human iPS	None reported	C>T mutation in potassium channel gene	Female	26 Years	Caucasian > European	No	No
UCSD247i-LQT1-2	Modified Human iPS	None reported	C>T mutation in potassium channel gene	Female	26 Years	Caucasian > European	No	No
UCSD243i-LQT3-1	Modified Human iPS	None reported	G>T mutation in sodium channel gene	Female	26 Years	Caucasian > European	No	No
UCSD244i-LQT3-2	Modified Human iPS	None reported	G>T mutation in sodium channel gene	Female	26 Years	Caucasian > European	No	No
UCSD245i-CNTL-1	Human iPS	None reported		Female	26 Years	Caucasian > European	No	No
UCSD246i-CNTL-2	Human iPS	None reported		Female	26 Years	Caucasian > European	No	No
EIFIIIi002-A	Human iPS	EIF3F-Related Neurodevelopmental Disorder	Whole exome sequencing revealed an autosomal recessive homozygous pathogenic variant in the EIF3F gene: c.694T>G/p.(Phe232Val)	Male	2 years	Caucasian > European	No	No

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