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Cellosaurus QBRIi017-A (CVCL_C1VY)

[Text version]
Cell line name QBRIi017-A
Synonyms CtrlM; hiPSC_11080402_c1
Accession CVCL_C1VY
Resource Identification Initiative To cite this cell line use: QBRIi017-A (RRID:CVCL_C1VY)
Comments From: Qatar Biomedical Research Institute; Doha; Quatar.
Population: Arab.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:15751; NAPB; Simple; c.354+2T>G; Zygosity=Heterozygous; Note=Splice donor mutation (PubMed=36272305).
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 63Y
Category Induced pluripotent stem cell
Publications

PubMed=36272305; DOI=10.1016/j.scr.2022.102943
Ali G., Habbab W., Alkhadairi G., Al-Shaban F.A., Stanton L.W.
Generation of induced pluripotent stem cell lines from nonaffected parents and monozygotic triplets affected with autism spectrum disorder and epilepsy.
Stem Cell Res. 65:102943-102943(2022)

Cross-references
Cell line databases/resources hPSCreg; QBRIi017-A
Biological sample resources BioSamples; SAMEA111396559
Encyclopedic resources Wikidata; Q114312748
Entry history
Entry creation22-Sep-2022
Last entry update19-Dec-2024
Version number6