Home  |  Contact

Cellosaurus MCRIi001-A-1 (CVCL_WN06)

[Text version]

Cell line name MCRIi001-A-1
Synonyms MCRIi001-A-OI26; PB001-OI26
Accession CVCL_WN06
Resource Identification Initiative To cite this cell line use: MCRIi001-A-1 (RRID:CVCL_WN06)
Comments From: Murdoch Children's Research Institute; Melbourne; Australia.
Population: Caucasian.
Derived from sampling site: Peripheral blood.
Sequence variations Heterozygous for COL1A1 p.Val1324Cysfs (c.3969dupT) (c.3969_3970insT); by CRISPR/Cas9 (PubMed=31075690).
Disease Osteogenesis imperfecta (NCIt: C26837)
Osteogenesis imperfecta (ORDO: Orphanet_666)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_UK82 (MCRIi001-A)
Sex of cell Male
Age at sampling 61Y
Category Induced pluripotent stem cell

PubMed=31075690; DOI=10.1016/j.scr.2019.101449
Hosseini Far H., Patria Y.N., Motazedian A., Elefanty A.G., Stanley E.G., Lamande S.R., Bateman J.F.
Generation of a heterozygous COL1A1 (c.3969_3970insT) osteogenesis imperfecta mutation human iPSC line, MCRIi001-A-1, using CRISPR/Cas9 editing.
Stem Cell Res. 37:101449-101449(2019)

Cell line databases/resources hPSCreg; MCRIi001-A-1
Biological sample resources BioSamples; SAMEA5873307
Other Wikidata; Q95986992
Entry history
Entry creation24-May-2019
Last entry update02-Jul-2020
Version number4