Home  |  Contact

Cellosaurus UKKi035-A (CVCL_VF42)

[Text version]

Cell line name UKKi035-A
Synonyms NP0139-A; NP0139-3E
Accession CVCL_VF42
Resource Identification Initiative To cite this cell line use: UKKi035-A (RRID:CVCL_VF42)
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_VF43 ! UKKi035-B
CVCL_VF44 ! UKKi035-C
Sex of cell Male
Age at sampling 65-69Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections EBiSC; UKKi035-A
ECACC; 66540895
Cell line databases/resources hPSCreg; UKKi035-A
Biological sample resources BioSamples; SAMEA104615859
Encyclopedic resources Wikidata; Q54990541
Entry history
Entry creation14-May-2018
Last entry update20-May-2021
Version number8