Cellosaurus GM27615 (CVCL_A2QS)
| Cell line name | GM27615 | |
|---|---|---|
| Accession | CVCL_A2QS | |
| Resource Identification Initiative | To cite this cell line use: GM27615 (RRID:CVCL_A2QS) | |
| Comments | Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. | |
| Sequence variations |
| |
| Disease | Rett syndrome, congenital variant (NCIt: C176903) Atypical Rett syndrome (ORDO: Orphanet_3095) | |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | |
| Hierarchy | Children:
| |
| Sex of cell | Male | |
| Age at sampling | 5Y | |
| Category | Finite cell line | |
| Cross-references | ||
| Cell line collections (Providers) | Coriell; GM27615 | |
| Encyclopedic resources | Wikidata; Q105507203 | |
| Entry history | ||
| Entry creation | 12-Jan-2021 | |
| Last entry update | 19-Dec-2024 | |
| Version number | 7 | |