Cellosaurus NH50359 (CVCL_B6HN)
| Cell line name | NH50359 |
|---|---|
| Accession | CVCL_B6HN |
| Resource Identification Initiative | To cite this cell line use: NH50359 (RRID:CVCL_B6HN) |
| Comments | Population: Caucasian. Characteristics: Non-edited control for NH50329 (Cellosaurus=CVCL_B6HM). 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_W577 (ND36999) |
| Sex of cell | Male |
| Age at sampling | 6Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | NHCDR; NH50359 |
| Encyclopedic resources | Wikidata; Q112129455 |
| Entry history | |
| Entry creation | 17-Mar-2022 |
| Last entry update | 19-Dec-2024 |
| Version number | 6 |