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Cellosaurus MCRIi019-A (CVCL_A9XY)

[Text version]
Cell line name MCRIi019-A
Synonyms 1502; 1502.3; MCRIAi001-A
Accession CVCL_A9XY
Resource Identification Initiative To cite this cell line use: MCRIi019-A (RRID:CVCL_A9XY)
Comments From: Murdoch Children's Research Institute; Melbourne; Australia.
Population: African American.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_2766 (WS1)
Children:
CVCL_A4WY (MCRIi019-A-1)CVCL_A9XZ (MCRIi019-A-2)CVCL_D0HS (MCRIi019-A-5)
CVCL_D0HR (MCRIi019-A-6)CVCL_A1QP (MCRIi019-A-7)
Sex of cell Female
Age at sampling 12FW
Category Induced pluripotent stem cell
Publications

PubMed=33002832; DOI=10.1016/j.scr.2020.101962
Kung L.H.-W., Sampurno L., Yammine K.M., Graham A., McDonald P., Bateman J.F., Shoulders M.D., Lamande S.R.
CRISPR/Cas9 editing to generate a heterozygous COL2A1 p.G1170S human chondrodysplasia iPSC line, MCRIi019-A-2, in a control iPSC line, MCRIi019-A.
Stem Cell Res. 48:101962-101962(2020)

PubMed=33316599; DOI=10.1016/j.scr.2020.102118
Kung L.H.-W., Sampurno L., Little C.B., Lamande S.R., Bateman J.F.
Generation of a miR-26b stem-loop knockout human iPSC line, MCRIi019-A-1, using CRISPR/Cas9 editing.
Stem Cell Res. 50:102118-102118(2021)

PubMed=34543885; DOI=10.1016/j.scr.2021.102515
Lilianty J., Bateman J.F., Lamande S.R.
Generation of a heterozygous COL2A1 (p.G1113C) hypochondrogenesis mutation iPSC line, MCRIi019-A-7, using CRISPR/Cas9 gene editing.
Stem Cell Res. 56:102515-102515(2021)

Cross-references
Cell line databases/resources hPSCreg; MCRIi019-A
Encyclopedic resources Wikidata; Q102114510
Entry history
Entry creation29-Oct-2020
Last entry update05-Oct-2023
Version number8