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Cellosaurus UKKi035-C (CVCL_VF44)

[Text version]

Cell line name UKKi035-C
Synonyms NP0139-C; NP0139-24D
Accession CVCL_VF44
Resource Identification Initiative To cite this cell line use: UKKi035-C (RRID:CVCL_VF44)
Comments From: Institute for Neurophysiology, Medical Faculty, University of Cologne; Cologne; Germany.
Derived from sampling site: Peripheral blood.
Sequence variations
  • Mutation; HGNC; 7551; MYBPC3; Simple; p.Arg943Ter (c.2827C>T); ClinVar=VCV000037039; Zygosity=Heterozygous (hPSCreg).
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_VF43 ! UKKi035-B
Sex of cell Male
Age at sampling 65-69Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections EBiSC; UKKi035-C
ECACC; 66540897
Cell line databases/resources hPSCreg; UKKi035-C
Biological sample resources BioSamples; SAMEA104615861
Encyclopedic resources Wikidata; Q54990544
Entry history
Entry creation14-May-2018
Last entry update20-May-2021
Version number8