Cellosaurus DD0102 (CVCL_8U69)
| Cell line name | DD0102 |
|---|---|
| Accession | CVCL_8U69 |
| Resource Identification Initiative | To cite this cell line use: DD0102 (RRID:CVCL_8U69) |
| Comments | Part of: ECACC chromosomal abnormality collection. Derived from site: In situ; Chorionic villus; UBERON=UBERON_0007106. |
| Disease | Fragile X syndrome (NCIt: C84717) Fragile X syndrome (ORDO: Orphanet_908) |
| 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; 89021601 |
| Encyclopedic resources | Wikidata; Q54828755 |
| Entry history | |
| Entry creation | 23-Feb-2016 |
| Last entry update | 29-Jun-2023 |
| Version number | 6 |