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Cellosaurus CPGHi006-A (CVCL_B5QR)

[Text version]
Cell line name CPGHi006-A
Synonyms PLAFMCi006-A
Accession CVCL_B5QR
Secondary accession CVCL_B6XG
Resource Identification Initiative To cite this cell line use: CPGHi006-A (RRID:CVCL_B5QR)
Comments From: Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital; Beijing; China.
Population: Chinese.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 9009; PKD2; Unexplicit; Ex3-15del; Zygosity=Heterozygous (PubMed=35091308).
Disease Autosomal dominant polycystic kidney disease (NCIt: C84578)
Autosomal dominant polycystic kidney disease (ORDO: Orphanet_730)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 42Y
Category Induced pluripotent stem cell
Publications

PubMed=35091308; DOI=10.1016/j.scr.2022.102681
Ma Y.-X., Shang S.-L., Shi M.-H., Yang Y.-Z., Li Q.-G., Bai X.-Y.
Establishment of the induced pluripotent stem cell line PLAFMCi006-A from peripheral blood mononuclear cells of polycystic kidney disease patients with PKD2 gene mutation.
Stem Cell Res. 60:102681-102681(2022)

Cross-references
Cell line databases/resources hPSCreg; CPGHi006-A
Biological sample resources BioSamples; SAMEA12123062
Encyclopedic resources Wikidata; Q111733134
Entry history
Entry creation17-Mar-2022
Last entry update29-Jun-2023
Version number5