Cellosaurus MYB#2.2 corrected (CVCL_E7AG)
Cell line name | MYB#2.2 corrected |
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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 |
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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) |
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 |
Entry history | |
Entry creation | 10-Apr-2025 |
Last entry update | 10-Apr-2025 |
Version number | 1 |