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Cell Line | Cell Line Alias | Cell Type | Disease | Genetic Alteration/Mutation | Sex | Age at Collection | Ethnicity | Genetically Related Cell Lines | dbGaP Data |
|---|---|---|---|---|---|---|---|---|---|
H1 | Human ES | None reported | Male | No | No | ||||
H9 | Human ES | None reported | Female | No | No | ||||
H14 | Human ES | None reported | Male | No | No | ||||
SC13-049; PCBC16hsi2013040201 | Human iPS | None reported | Male | Adult | Unknown | No | No | ||
DCX Cit/Y | Modified Human ES | None reported | Male | No | No | ||||
SOX2 Cit/+ | Modified Human ES | None reported | Male | No | No | ||||
Modified Human ES | Timothy Syndrome | Point mutation introduced into both alleles of the CACNA1C gene. Mutation of Gly406 to Arg (G406R) was introduced. | Male | No | No | ||||
PAX6 Cit/+ | Modified Human ES | None reported | Male | No | No | ||||
Modified Human ES | 16p11.2 disorders | Disruption of one allele of KCTD13. | Male | No | No | ||||
Modified Human ES | 16p11.2 disorders | Disruption of both alleles of KCTD13. | Male | No | No |