Cell Line Search

Showing 1489–1504 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
PACSIIi002-A		Human iPS	PACS2 Syndrome	Whole exome sequencing revealed a de novo autosomal dominant heterozygous pathogenic variant in the PACS2 gene: p.Glu209Lys/p.E209K (c.625G>A)	Male	9 years	Caucasian	No	No
PACSIIi003-A		Human iPS	PACS2 Syndrome	Whole exome sequencing revealed a de novo autosomal dominant heterozygous pathogenic variant in the PACS2 gene: p.Glu209Lys/p.E209K (c.625G>A)	Female	3 years	Caucasian	No	No
CVCL_C7V6	WIBR3_EWT_S6	Human ES	None Reported		Female			No	No
CVCL_C7V4	WIBR3_EWT_S4	Human ES	None Reported		Female			No	No
CVCL_C7V1	WIBR3_EWT_S1	Human ES	None Reported		Female			No	No
CVCL_C7VY	WIBR3_SNCA_A53T_4	Modified Human ES	Parkinson's disease	SNCA A53T, NP_000336.1 p.A53T/WT	Female			No	No
CVCL_C7V3	WIBR3_EWT_S3	Modified Human ES	None Reported		Female			No	No
CVCL_C7VW	WIBR3_SNCA_A53T_1	Modified Human ES	Parkinson's disease	SNCA A53T, NP_000336.1, p.A53T/WT	Female			No	No
CVCL_C7VG	WIBR3_LRRK2_G2019S_5_Het	Modified Human ES	Parkinson's disease	LRRK2 G2019S, NP_940980.4, p.G2019S/WT	Female			No	No
CVCL_D3YC	WIBR3_LRRK2_G2019S_2093_Het	Modified Human ES	Parkinson's disease	LRRK2 G2019S, NP_940980.4, p.G2019S/WT	Female			No	No