Cellosaurus DD1735 (CVCL_9H29)
| Cell line name | DD1735 |
|---|---|
| Accession | CVCL_9H29 |
| Resource Identification Initiative | To cite this cell line use: DD1735 (RRID:CVCL_9H29) |
| Comments | Part of: ECACC chromosomal abnormality collection. Karyotypic information: 46,XX [59]; 47,XX,+mar [6] (ECACC=94012815). Derived from site: In situ; Fetus; UBERON=UBERON_0000323. Cell type: Fibroblast; CL=CL_0000057. |
| Disease | Congenital heart disease (NCIt: C95834) Rare syndrome with cardiac malformations (ORDO: Orphanet_156532) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Female |
| Age at sampling | Fetus |
| Category | Finite cell line |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 94012815 |
| Encyclopedic resources | Wikidata; Q54829945 |
| Entry history | |
| Entry creation | 23-Feb-2016 |
| Last entry update | 29-Jun-2023 |
| Version number | 7 |