Cellosaurus WC007i-FX13-2 (CVCL_EJ78)
| Cell line name | WC007i-FX13-2 | |
|---|---|---|
| Synonyms | FX13-2 | |
| Accession | CVCL_EJ78 | |
| Resource Identification Initiative | To cite this cell line use: WC007i-FX13-2 (RRID:CVCL_EJ78) | |
| Comments | Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. | |
| Sequence variations |
| |
| Disease | Fragile X syndrome (NCIt: C84717) Fragile X syndrome (ORDO: Orphanet_908) | |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | |
| Hierarchy | Children:
| |
| Sex of cell | Male | |
| Age at sampling | 8Y | |
| Category | Induced pluripotent stem cell | |
| Publications | PubMed=24654675; DOI=10.1089/scd.2014.0030; PMCID=PMC4103262 | |
| Cross-references | ||
| Cell line collections (Providers) | WiCell; wc007i-fx13-2 | |
| Encyclopedic resources | Wikidata; Q54993618 | |
| Entry history | ||
| Entry creation | 26-Sep-2016 | |
| Last entry update | 29-Jun-2023 | |
| Version number | 12 | |