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Cellosaurus IBBISTi010-A (CVCL_E4D2)

[Text version]
Cell line name IBBISTi010-A
Synonyms 4_H17
Accession CVCL_E4D2
Resource Identification Initiative To cite this cell line use: IBBISTi010-A (RRID:CVCL_E4D2)
Comments From: Simao Jose Teixeira da Rocha; Porto Salvo; Portugal.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:7551; MYBPC3; Simple; c.1224-52G>A; ClinVar=VCV000188544; Zygosity=Heterozygous (hPSCreg; IBBISTi010-A).
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)
Sex of cell Female
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; IBBISTi010-A
Biological sample resources BioSamples; SAMEA115861649
Entry history
Entry creation19-Dec-2024
Last entry update19-Dec-2024
Version number1