| Cell line name | CHDIi026-A |
|---|---|
| Synonyms | #26C3; #26c3; CHDI-90002174 |
| Accession | CVCL_VC97 |
| Resource Identification Initiative | To cite this cell line use: CHDIi026-A (RRID:CVCL_VC97) |
| Comments | From: CHDI Foundation; New York; USA. Miscellaneous: At sampling donor was not affected with Huntington disease but at significant risk for disease. Derived from sampling site: Cell type=Fibroblast. |
| Sequence variations | Mutation; HGNC; 4851; HTT; Repeat_expansion; p.Gln18[47] (c.52CAG(47)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (EBiSC). |
| Disease | Huntington's disease (NCIt: C82342) Huntington disease (ORDO: Orphanet_399) |
| Species of origin | Homo sapiens (Human)
(NCBI Taxonomy: 9606)
|
| Sex of cell | Female |
| Age at sampling | 30-34Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections | EBiSC; CHDIi026-A
ECACC; 66541158 |
| Cell line databases/resources | hPSCreg; CHDIi026-A |
| Biological sample resources | BioSamples; SAMEA1088047 |
| Encyclopedic resources | Wikidata; Q54811793 |
| Entry history | |
| Entry creation | 14-May-2018 |
| Last entry update | 16-Dec-2021 |
| Version number | 7 |