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Cellosaurus MYB#2.2 corrected (CVCL_E7AG)

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Cell line name MYB#2.2 corrected
Synonyms IsoMYB2#2 clone 2
Accession CVCL_E7AG
Resource Identification Initiative To cite this cell line use: MYB#2.2 corrected (RRID:CVCL_E7AG)
Comments From: Centro de Medecina Regenerativa de Barcelona (CMRB); Barcelona; Spain.
Derived from site: In situ; Arm, skin, dermis; UBERON=UBERON_0002427+UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:7551; MYBPC3; Simple_corrected; p.Lys600Asnfs*2 (c.1800delA); ClinVar=VCV000042568; Zygosity=Heterozygous; Note=By CRISPR/Cas9 (PubMed=37317833).
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)
Hierarchy Parent: CVCL_E7AE (MYB#2.2)
Sex of cell Female
Age at sampling 36Y
Category Induced pluripotent stem cell
Publications

PubMed=37317833; DOI=10.1161/CIRCRESAHA.122.321951
Ruben Escriba, Jose Maria Larranaga-Moreira, Yvonne Richaud-Patin, Lea Pourchet, Ioannis Lazis, Senda Jimenez-Delgado, Alba Morillas-Garcia, Martin Ortiz-Genga, Juan Pablo Ochoa, David Carreras Gorgals, Guillermo Javier Perez ...Show all 16 authors... , Jose Luis de la Pompa, Ramon Brugada, Lorenzo Monserrat, Roberto Barriales-Villa, Angel Raya; Show fewer authors
iPSC-based modeling of variable clinical presentation in hypertrophic cardiomyopathy.
Circ. Res. 133:108-119(2023)

Entry history
Entry creation10-Apr-2025
Last entry update10-Apr-2025
Version number1