Cellosaurus DD2135 (CVCL_9I99)
| Cell line name | DD2135 |
|---|---|
| Accession | CVCL_9I99 |
| Resource Identification Initiative | To cite this cell line use: DD2135 (RRID:CVCL_9I99) |
| Comments | Part of: ECACC chromosomal abnormality collection. Karyotypic information: 47,XYY (ECACC=94112416). Derived from site: In situ; Fetal muscle; UBERON=UBERON_0001630. Cell type: Fibroblast of muscle; CL=CL_1001609. |
| Disease | 47,XYY syndrome (NCIt: C85237) 47,XYY syndrome (ORDO: Orphanet_8) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_9I85 ! DD2111 |
| Sex of cell | Male |
| Age at sampling | Fetus |
| Category | Finite cell line |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 94112416 |
| Encyclopedic resources | Wikidata; Q54830132 |
| Entry history | |
| Entry creation | 23-Feb-2016 |
| Last entry update | 29-Jun-2023 |
| Version number | 7 |