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Cellosaurus UKKi025-B (CVCL_LD43)

[Text version]

Cell line name UKKi025-B
Synonyms NP0135-2
Accession CVCL_LD43
Resource Identification Initiative To cite this cell line use: UKKi025-B (RRID:CVCL_LD43)
Comments From: Institute for Neurophysiology, Medical Faculty, University of Cologne; Cologne; Germany.
Population: Caucasian.
Derived from sampling site: Peripheral blood.
Sequence variations
  • Mutation; HGNC; 7577; MYH7; Simple; p.Arg719Gly (c.2156G>A); Zygosity=Heterozygous (EBiSC).
Disease Familial hypertrophic cardiomyopathy type 1 (NCIt: C172092)
Rare familial disorder with hypertrophic cardiomyopathy (ORDO: Orphanet_99739)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_LD42 ! UKKi025-A
CVCL_LD44 ! UKKi025-C
Sex of cell Female
Age at sampling 40-44Y
Category Induced pluripotent stem cell
Cell line collections EBiSC; UKKi025-B
ECACC; 66540492
Cell line databases/resources hPSCreg; UKKi025-B
Biological sample resources BioSamples; SAMEA17638168
Encyclopedic resources Wikidata; Q54990491
Entry history
Entry creation22-Aug-2017
Last entry update20-May-2021
Version number9