Cellosaurus DD2108 (CVCL_9I82)
| Cell line name | DD2108 |
|---|---|
| Accession | CVCL_9I82 |
| Resource Identification Initiative | To cite this cell line use: DD2108 (RRID:CVCL_9I82) |
| Comments | Part of: ECACC chromosomal abnormality collection. Karyotypic information: 47,XX,+18 (ECACC=94102502). Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Holoprosencephaly (NCIt: C74988) Trisomy 18 (NCIt: C36626) Holoprosencephaly (ORDO: Orphanet_2162) Trisomy 18 (ORDO: Orphanet_3380) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Male |
| Age at sampling | Fetus |
| Category | Finite cell line |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 94102502 |
| Encyclopedic resources | Wikidata; Q54830115 |
| Entry history | |
| Entry creation | 23-Feb-2016 |
| Last entry update | 29-Jun-2023 |
| Version number | 6 |