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Cellosaurus UKKi035-B (CVCL_VF43)

[Text version]
Cell line name UKKi035-B
Synonyms NP0139-B; NP0139-6C
Accession CVCL_VF43
Resource Identification Initiative To cite this cell line use: UKKi035-B (RRID:CVCL_VF43)
Comments From: Institute for Neurophysiology, Medical Faculty, University of Cologne; Cologne; Germany.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 7551; MYBPC3; Simple; p.Arg943Ter (c.2827C>T); ClinVar=VCV000037039; Zygosity=Heterozygous (hPSCreg=UKKi035-B).
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_VF42 ! UKKi035-A
CVCL_VF44 ! UKKi035-C
Sex of cell Male
Age at sampling 65-69Y
Category Induced pluripotent stem cell
Cell line collections (Providers) EBiSC; UKKi035-B
ECACC; 66540896 - Discontinued
Cell line databases/resources hPSCreg; UKKi035-B
Biological sample resources BioSamples; SAMEA104615860
Encyclopedic resources Wikidata; Q54990542
Entry history
Entry creation14-May-2018
Last entry update30-Jan-2024
Version number11