Cell Line Identifier	Alternative Names	Maintainer	Producer	Parental Cell Type	Tissue of Origin	Disease as reported	Modified?	Curation Status	Related Lines
MCRIi001-A-2	—	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	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	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	Lamandé	Murdoch Children's Research Institute	—	—	spondyloepiphyseal dysplasia congenita	True	Not yet reviewed by Australian Stem Cell Registry	—
MCRIi019-A	1502; 1502.3	Lamandé	Murdoch Children's Research Institute	fibroblast	—	—	False	Not yet reviewed by Australian Stem Cell Registry	—
MCRIi019-A-2	COL2A1 p.G1170S; 1502-COL2A1p.G1170S; 1502.3 COL2A1 p.G1170S	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	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	Lamandé	Murdoch Children's Research Institute	—	—	achondrogenesis type ii	True	Not yet reviewed by Australian Stem Cell Registry	—