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Cellosaurus KSCBi006-A (CVCL_WR18)

[Text version]
Cell line name KSCBi006-A
Synonyms KNIH-OI001i-A
Accession CVCL_WR18
Resource Identification Initiative To cite this cell line use: KSCBi006-A (RRID:CVCL_WR18)
Comments From: National Institute of Health, Korea-National Stem Cell Bank (KSCB); Cheongwon-gun; South Korea.
Population: Asian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 2197; COL1A1; Simple; p.Gly1055Alafs*53 (c.3162delT); ClinVar=VCV000285398; Zygosity=Unspecified (PubMed=31715426).
HLA typing Source: PubMed=31715426
Class I
HLA-AA*24:02,24:02
HLA-BB*15:01,54:01
Class II
HLA-DRDRB1*04:03,15:01
Disease Osteogenesis imperfecta (NCIt: C26837)
Osteogenesis imperfecta (ORDO: Orphanet_666)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 10Y
Category Induced pluripotent stem cell
Publications

PubMed=31715426; DOI=10.1016/j.scr.2019.101622
Kim B.-Y., Ko J.M., Park M.-H., Koo S.K.
Generation of a patient-specific induced pluripotent stem cell line, KSCBi006-A, for osteogenesis imperfecta type I with the COL1A1, c.3162delT mutation.
Stem Cell Res. 41:101622-101622(2019)

Cross-references
Cell line databases/resources hPSCreg; KSCBi006-A
SKIP; SKIP005598
Biological sample resources BioSamples; SAMEA5712217
Encyclopedic resources Wikidata; Q95980260
Entry history
Entry creation05-Jul-2019
Last entry update29-Jun-2023
Version number9