Cell Line Identifier Alternative Names Maintainer Producer Parental Cell Type Tissue of Origin Disease as reported Modified? Curation Status Related Lines
MCRIi001-A-2 — Shireen Lamandé Murdoch Children's Research Institute erythroblast — — True Not yet reviewed by Australian Stem Cell Registry —
MCRIi001-A-3 TRPV4 p.F273L; MCRIi001-A-2-TRPV4 p.F273L; PB001-SOX9tdTom-TRPV4p.F273L; SOX9tdTom-TRPV4 p.F273L Shireen Lamandé Murdoch Children's Research Institute erythroblast — familial digital arthropathy-brachydactyly True Not yet reviewed by Australian Stem Cell Registry —
MCRIi001-A-4 TRPV4 p.P799L; MCRIi001-A-2-TRPV4 p.P799L; PB001-SOX9tdTOM-TRPV4pP799L; SOX9tdTom TRPV4 p.P799L Shireen Lamandé Murdoch Children's Research Institute erythroblast — metatropic dysplasia True Not yet reviewed by Australian Stem Cell Registry —
MCRIi001-B COL2A1 p.R989C; MCRIi001-A-SOX9tdTom-COL2A1p.R989C; PB001-SOX9tdTom-COL2A1p.R989C Shireen Lamandé Murdoch Children's Research Institute — — spondyloepiphyseal dysplasia congenita True Not yet reviewed by Australian Stem Cell Registry —
MCRIi019-A 1502; 1502.3 Shireen Lamandé Murdoch Children's Research Institute fibroblast — — False Flagged for further review —
MCRIi019-A-2 COL2A1 p.G1170S; 1502-COL2A1p.G1170S; 1502.3 COL2A1 p.G1170S Shireen Lamandé Murdoch Children's Research Institute — — legg-calve-perthes disease True Not yet reviewed by Australian Stem Cell Registry —
MCRIi019-A-6 COL2A1 p.R719C; 1502.3 COL2A1 p.R719C; 1502-COL2A1 p.R719C Shireen Lamandé Murdoch Children's Research Institute — — mild spondyloepiphyseal dysplasia due to col2a1 mutation with early-onset osteoarthritis True Not yet reviewed by Australian Stem Cell Registry —
MCRIi019-A-7 COL2A1 p.G1113C; 1502.3 COL2A1 p.G1113C; 1502-COL2A1 p.G1113C Shireen Lamandé Murdoch Children's Research Institute — — achondrogenesis type ii True Not yet reviewed by Australian Stem Cell Registry —