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Cellosaurus IBBISTi008-B (CVCL_D6M1)

[Text version]
Cell line name IBBISTi008-B
Synonyms F82 clone 3; 3F82; 128_3
Accession CVCL_D6M1
Resource Identification Initiative To cite this cell line use: IBBISTi008-B (RRID:CVCL_D6M1)
Comments From: Instituto de Medicina Molecular Joao Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa; Lisboa; Portugal.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
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)
Originate from same individual CVCL_D6M0 ! IBBISTi008-A
Sex of cell Female
Age at sampling 43Y
Category Induced pluripotent stem cell
Publications

PubMed=38417376; DOI=10.1016/j.scr.2024.103362
Marta Ribeiro, Joanna Jager, Marta Furtado, Teresa Carvalho, Joaquim Manuel Sampaio Cabral, Dulce Brito, Maria do Carmo-Fonseca, Sandra Martins, Simao Jose Teixeira da Rocha;
Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying MYBPC3 nonsense mutations.
Stem Cell Res. 76:103362-103362(2024)

Cross-references
Cell line databases/resources hPSCreg; IBBISTi008-B
Biological sample resources BioSamples; SAMEA115165747
Encyclopedic resources Wikidata; Q127382080
Entry history
Entry creation02-May-2024
Last entry update14-Aug-2025
Version number4