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Cellosaurus UKBi015-A-7 (CVCL_E8WM)

[Text version]
Cell line name UKBi015-A-7
Synonyms iLB-C16bm-s6 edit BAG3 E10
Accession CVCL_E8WM
Resource Identification Initiative To cite this cell line use: UKBi015-A-7 (RRID:CVCL_E8WM)
Comments From: Institut fur Rekonstruktive Neurobiologie, University Clinic of Bonn; Bonn; Germany.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:939; BAG3; Simple_edited; p.Pro209Leu (c.626C>T); ClinVar=VCV000005981; Zygosity=Heterozygous; Note=By CRISPR/Cas9 (hPSCreg=UKBi015-A-7).
Disease Myofibrillar myopathy 6 (NCIt: C217088)
Muscular dystrophy, Selcen type (ORDO: Orphanet_199340)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_A9Q8 (UKBi015-A)
Sex of cell Male
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; UKBi015-A-7
Biological sample resources BioSamples; SAMEA115753181
Entry history
Entry creation14-Aug-2025
Last entry update14-Aug-2025
Version number1