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Cellosaurus CBRCULi016-A (CVCL_D1FY)

[Text version]
Cell line name CBRCULi016-A
Synonyms SCN5A p.R219H-14C; SCN5A p.R219H clone 14C
Accession CVCL_D1FY
Resource Identification Initiative To cite this cell line use: CBRCULi016-A (RRID:CVCL_D1FY)
Comments From: CERVO Brain Research Centre, Universite Laval; Quebec; Canada.
Population: Caucasian.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Brugada syndrome (NCIt: C142891)
Brugada syndrome (ORDO: Orphanet_130)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_D1FZ (CBRCULi016-A-1)
Sex of cell Male
Age at sampling 29Y
Category Induced pluripotent stem cell
Publications

PubMed=38232626; DOI=10.1016/j.scr.2024.103308
Djemai M., Jauvin D., Poulin H., Chapotte-Baldacci C.-A., Chahine M.
Generation of a patient-specific iPSC cell line with cardiac arrhythmias and dilated cardiomyopathy (CBRCULi016-A), an isogenic control (CBRCULi016-A-1), and a paternal control (CBRCULi017-A).
Stem Cell Res. 75:103308-103308(2024)

Cross-references
Cell line databases/resources hPSCreg; CBRCULi016-A
Biological sample resources BioSamples; SAMEA114425089
Encyclopedic resources Wikidata; Q127380402
Entry history
Entry creation30-Jan-2024
Last entry update19-Dec-2024
Version number4