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Cellosaurus HCM HJ 1-n (CVCL_T926)

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Cell line name HCM HJ 1-n
Accession CVCL_T926
Resource Identification Initiative To cite this cell line use: HCM HJ 1-n (RRID:CVCL_T926)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:7551; MYBPC3; Simple; p.Gly999_Gln1004del; Zygosity=Unspecified (PubMed=25389285).
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_T925 ! HCM HJ 1-i
Sex of cell Female
Age at sampling 45Y
Category Induced pluripotent stem cell
Publications

PubMed=25389285; DOI=10.1161/JAHA.114.001263; PMCID=PMC4338713
Atsushi Tanaka, Shinsuke Yuasa, Giulia Mearini, Toru Egashira, Tomohisa Seki, Masaki Kodaira, Dai Kusumoto, Yusuke Kuroda, Shinichiro Okata, Tomoyuki Suzuki, Taku Inohara ...Show all 19 authors... , Takuro Arimura, Shinji Makino, Kensuke Kimura, Akinori Kimura, Tetsushi Furukawa, Lucie Carrier, Koichi Node, Keiichi Fukuda; Show fewer authors
Endothelin-1 induces myofibrillar disarray and contractile vector variability in hypertrophic cardiomyopathy-induced pluripotent stem cell-derived cardiomyocytes.
J. Am. Heart Assoc. 3:e001263.1-e001263.25(2014)

Cross-references
Cell line databases/resources SKIP; SKIP000212 - Discontinued
Encyclopedic resources Wikidata; Q54881886
Entry history
Entry creation03-Feb-2014
Last entry update19-Dec-2024
Version number10