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Cellosaurus SCVIi067-A (CVCL_C1SE)

[Text version]
Cell line name SCVIi067-A
Synonyms SCVI-2742; SCVI 2742; SCVI2742
Accession CVCL_C1SE
Resource Identification Initiative To cite this cell line use: SCVIi067-A (RRID:CVCL_C1SE)
Comments From: Stanford Cardiovascular Institute; Palo Alto; USA.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 12405; TTR; Simple; p.Val50Met (c.148G>A) (V30M); dbSNP=rs28933979; Zygosity=Heterozygous (PubMed=37788558).
Disease Hereditary transthyretin amyloid cardiomyopathy (NCIt: C165489)
ATTRV30M amyloidosis (ORDO: Orphanet_85447)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 63Y
Category Induced pluripotent stem cell
Publications

PubMed=37788558; DOI=10.1016/j.scr.2023.103215; PMCID=PMC10821799
Bonilauri B., Shin H.S., Htet M.H., Yan C.D., Witteles R.M., Sallam K., Wu J.C.
Generation of two induced pluripotent stem cell lines from patients with cardiac amyloidosis carrying heterozygous transthyretin (TTR) mutation.
Stem Cell Res. 72:103215-103215(2023)

Cross-references
Cell line databases/resources hPSCreg; SCVIi067-A
Biological sample resources BioSamples; SAMEA110424195
Encyclopedic resources Wikidata; Q114312981
Entry history
Entry creation22-Sep-2022
Last entry update30-Jan-2024
Version number5