Cell line name | ICGi029-A |
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Synonyms | HCM14fm6.2 |
Accession | CVCL_A5VV |
Resource Identification Initiative | To cite this cell line use: ICGi029-A (RRID:CVCL_A5VV) |
Comments | From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia. Population: Caucasian. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
Sequence variations |
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Disease | Familial hypertrophic cardiomyopathy type 4 (NCIt: C133725) Rare familial disorder with hypertrophic cardiomyopathy (ORDO: Orphanet_99739) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Sex of cell | Female |
Age at sampling | 65Y |
Category | Induced pluripotent stem cell |
Publications | PubMed=33892289; DOI=10.1016/j.scr.2021.102344 |
Cross-references | |
Cell line databases/resources | hPSCreg; ICGi029-A |
Biological sample resources | BioSamples; SAMEA8307096 |
Encyclopedic resources | Wikidata; Q107115426 |
Entry history | |
Entry creation | 20-May-2021 |
Last entry update | 29-Jun-2023 |
Version number | 4 |