| Cell line name | ND41113 |
|---|---|
| Synonyms | ND41113*D |
| Accession | CVCL_Y809 |
| Resource Identification Initiative | To cite this cell line use: ND41113 (RRID:CVCL_Y809) |
| Comments | Population: Caucasian. Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
|
| Disease | Huntington's disease (NCIt: C82342) Huntington disease (ORDO: Orphanet_399) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_W557 (GM02183) |
| Sex of cell | Female |
| Age at sampling | 21Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | Coriell; ND41113 - Discontinued
NHCDR; ND41113 |
| Cell line databases/resources | SKIP; SKIP001555
SKIP; SKIP004720 |
| Encyclopedic resources | Wikidata; Q54930193 |
| Entry history | |
| Entry creation | 10-Apr-2015 |
| Last entry update | 30-Jan-2024 |
| Version number | 15 |