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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 |
|---|---|---|---|---|---|---|---|---|---|
TSC2-/- | Modified Human iPS | Tuberous Sclerosis Complex | C972G/C972G | Male | 18 years | No | No | ||
IMR90-TSC2+/- | Modified Human iPS | Tuberous Sclerosis Complex | 972C/C972G | Female | No | No | |||
IMR90-TSC2-/- | Modified Human iPS | Tuberous Sclerosis Complex
| C972G/C972G
| Female | No | No | |||
WIBR3_PRKN_X3DEL_F2-5 | Modified Human ES | Parkinson's disease
| PRKN Exon 3 Deletion, NP_004553.2, p.N58Qfs*39/p.N58Qfs*39
| Female | No | No | |||
WIBR3_PINK1_Q129X_C4-1 | Modified Human ES | Parkinson's disease
| PINK1 Q129X, NP_115785.1, p.Q129X/p.Q129X
| Female | No | No | |||
CVCL_C8BF | Human ES | None Reported
| Female | No | No | ||||
CVCL_C8BD | Human ES | None Reported
| Female | No | No | ||||
CVCL_C8BE | Human ES | None Reported
| Female | No | No | ||||
WIBR3_PRKN_X3DEL_B1-3 | Modified Human ES | Parkinson's disease
| PRKN Exon 3 Deletion, NP_004553.2, p.N58Qfs*39/p.N58Qfs*39
| Female | No | No | |||
WIBR3_FBXO7_FS_A3-1 | Modified Human ES | Parkinson's disease
| FBXO7 Frameshift, NP_036311.3, p.R498Efs*27/p.R498Efs*27
| Female | No | No |