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Cellosaurus EURACi008-A (CVCL_A0LW)

[Text version]
Cell line name EURACi008-A
Synonyms PZG#4
Accession CVCL_A0LW
Resource Identification Initiative To cite this cell line use: EURACi008-A (RRID:CVCL_A0LW)
Comments From: EURAC Research Institute for Biomedicine; Bolzano; Italy.
Population: Caucasian.
Characteristics: While harboring the same PKP2 mutation as a family member from which EURACi007-A (Cellosaurus=CVCL_A0LV) was derived, the donor of this cell line did not show any symptom of arrhythmogenic right ventricular dysplasia.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:9024; PKP2; Simple; p.Asn346Leufs*12 (c.1035-5203_1171-13298del); Zygosity=Heterozygous (PubMed=34298432).
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 67Y
Category Induced pluripotent stem cell
Publications

PubMed=34298432; DOI=10.1016/j.scr.2021.102466
Meraviglia V., Cattelan G., De Bortoli M., Motta B.M., Volpato C.B., Frommelt L.-S., Rauhe W., Di Segni M., Silipigni R., Pramstaller P.P., Rossini A.
Generation and characterization of three human induced pluripotent stem cell lines (EURACi007-A, EURACi008-A, EURACi009-A) from three different individuals of the same family with arrhythmogenic cardiomyopathy (ACM) carrying the plakophillin2 p.N346Lfs*12 mutation.
Stem Cell Res. 55:102466-102466(2021)

Cross-references
Cell line databases/resources hPSCreg; EURACi008-A
Encyclopedic resources Wikidata; Q108820203
Entry history
Entry creation23-Sep-2021
Last entry update19-Dec-2024
Version number5