Cellosaurus ND36999 (CVCL_W577)
| Cell line name | ND36999 | ||
|---|---|---|---|
| Synonyms | ND36999*F; HD 6 | ||
| Accession | CVCL_W577 | ||
| Resource Identification Initiative | To cite this cell line use: ND36999 (RRID:CVCL_W577) | ||
| Comments | Population: Caucasian. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. | ||
| Sequence variations |
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| Disease | Huntington's disease (NCIt: C82342) Huntington disease (ORDO: Orphanet_399) | ||
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | ||
| Hierarchy | Parent: CVCL_W576 (GM09197) Children:
| ||
| Sex of cell | Male | ||
| Age at sampling | 6Y | ||
| Category | Induced pluripotent stem cell | ||
| Cross-references | |||
| Cell line collections (Providers) | Coriell; ND36999 - Discontinued
NHCDR; ND36999 | ||
| Cell line databases/resources | SKIP; SKIP001089
SKIP; SKIP004701 | ||
| Encyclopedic resources | Wikidata; Q54930008 | ||
| Entry history | |||
| Entry creation | 16-Apr-2014 | ||
| Last entry update | 19-Dec-2024 | ||
| Version number | 18 | ||