| Cell line name | UKKi025-A |
|---|---|
| Synonyms | NP0135-1 |
| Accession | CVCL_LD42 |
| Resource Identification Initiative | To cite this cell line use: UKKi025-A (RRID:CVCL_LD42) |
| Comments | From: Institute for Neurophysiology, Medical Faculty, University of Cologne; Cologne; Germany. Population: Caucasian. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Sequence variations |
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| Disease | Familial hypertrophic cardiomyopathy type 1 (NCIt: C172092) Rare familial disorder with hypertrophic cardiomyopathy (ORDO: Orphanet_99739) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_LD43 ! UKKi025-B CVCL_LD44 ! UKKi025-C |
| Sex of cell | Female |
| Age at sampling | 40-44Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | EBiSC; UKKi025-A
ECACC; 66540491 - Discontinued |
| Cell line databases/resources | hPSCreg; UKKi025-A |
| Biological sample resources | BioSamples; SAMEA17636668 |
| Encyclopedic resources | Wikidata; Q54990490 |
| Entry history | |
| Entry creation | 22-Aug-2017 |
| Last entry update | 30-Jan-2024 |
| Version number | 12 |