Cellosaurus CW20002 (CVCL_4Q71)
| Cell line name | CW20002 |
|---|---|
| Synonyms | CIRM-CW20002i-Affected; CIRMi13X-A |
| Accession | CVCL_4Q71 |
| Resource Identification Initiative | To cite this cell line use: CW20002 (RRID:CVCL_4Q71) |
| Comments | From: California Institute for Regenerative Medicine (CIRM); San Francisco; USA. Population: Caucasian. Donor information: Established from monozygotic twin of CW20042 (Cellosaurus=CVCL_4Q82). Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Autism spectrum disorder (NCIt: C88412) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Female |
| Age at sampling | 6Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | Coriell; CW20002 - Discontinued
FCDI; CW20002 |
| Cell line databases/resources | hPSCreg; CIRMi13X-A
SKIP; SKIP003661 |
| Biological sample resources | BioSamples; SAMEA115401904 |
| Encyclopedic resources | Wikidata; Q54815092 |
| Entry history | |
| Entry creation | 22-Sep-2015 |
| Last entry update | 02-May-2024 |
| Version number | 15 |