Cell Line Identifier Alternative Names Maintainer Producer Parental Cell Type Tissue of Origin Disease as reported Modified? Curation Status Related Lines
AIBNi009-A GENIE 49 Wolvetang Australian Institute for Bioengineering and Nanotechnology peripheral blood mononuclear cell — epilepsy False Not yet reviewed by Australian Stem Cell Registry —
AIBNi018-A SPGh2-S964pC6 Wolvetang Australian Institute for Bioengineering and Nanotechnology peripheral blood mononuclear cell — — False Not yet reviewed by Australian Stem Cell Registry —
FINi002-A FI.CPLT.PRKN.R275W+del_e8.PK006; PK6 C4 Parish The Florey Institute of Neuroscience and Mental Health fibroblast — parkinson disease False Not yet reviewed by Australian Stem Cell Registry —
FINi003-A FI.SPSM.SCN2A.E1211K.008; NGF008 c3 Petrou The Florey Institute of Neuroscience and Mental Health fibroblast — developmental and epileptic encephalopathy False Not yet reviewed by Australian Stem Cell Registry —
GENEAe010-A GENEA011; SIVF11; SIVF011 Schmidt Genea — — — False Not yet reviewed by Australian Stem Cell Registry —
GENEAe012-A GENEA013; SIVF13; SIV013 Schmidt Genea — — — False Not yet reviewed by Australian Stem Cell Registry —
GENEAe016-A GENEA022 Biocells Genea — — — False Not yet reviewed by Australian Stem Cell Registry —
GENEAe017-A GENEA023 Biocells Genea — — — False Not yet reviewed by Australian Stem Cell Registry —
GENEAe021-A GENEA021 Biocells Genea — — — False Not yet reviewed by Australian Stem Cell Registry —
HPIi005-A RYR1-5-9214-iPSC clone R5 Clayton Harry Perkins Institute of Medical Research LCL — central core myopathy False Not yet reviewed by Australian Stem Cell Registry —
HPIi005-B RYR1-5-9214-iPSC clone R11 Clayton Harry Perkins Institute of Medical Research LCL — central core myopathy False Not yet reviewed by Australian Stem Cell Registry —
HPIi006-A RYR1-3278-R2A Clayton Harry Perkins Institute of Medical Research LCL — central core myopathy False Not yet reviewed by Australian Stem Cell Registry —
HPIi009-A RYR1-15377-R1B Clayton Harry Perkins Institute of Medical Research LCL — central core myopathy False Not yet reviewed by Australian Stem Cell Registry —
HPIi010-A MYH7-17773-R4A Clayton Harry Perkins Institute of Medical Research LCL — myh7-related skeletal myopathy False Not yet reviewed by Australian Stem Cell Registry —
HPIi011-A MYH7-18681-R1A Clayton Harry Perkins Institute of Medical Research LCL — myh7-related skeletal myopathy False Not yet reviewed by Australian Stem Cell Registry —
HPIi012-A MYH7-19203-R1D Clayton Harry Perkins Institute of Medical Research LCL — myh7-related skeletal myopathy False Not yet reviewed by Australian Stem Cell Registry —
LEIi008-A 1093ips4 McLenachan Lions Eye Institute fibroblast — retinitis pigmentosa 11 False Not yet reviewed by Australian Stem Cell Registry —
LEIi012-A 1357ips5; 012-A McLenachan Lions Eye Institute fibroblast — stargardt disease False Not yet reviewed by Australian Stem Cell Registry —
LEIi012-B 1357iPS11; 012-B McLenachan Lions Eye Institute fibroblast — stargardt disease False Not yet reviewed by Australian Stem Cell Registry —
LEIi016-A 1418ips3 McLenachan Lions Eye Institute fibroblast — retinitis pigmentosa 12 False Not yet reviewed by Australian Stem Cell Registry —
LEIi016-B 1418ips6 McLenachan Lions Eye Institute fibroblast — retinitis pigmentosa 12 False Not yet reviewed by Australian Stem Cell Registry —
LEIi018-A 1607ips6 McLenachan Lions Eye Institute fibroblast — stargardt disease False Not yet reviewed by Australian Stem Cell Registry —
LEIi019-A 1020ips3 McLenachan Lions Eye Institute fibroblast — patterned dystrophy of the retinal pigment epithelium False Not yet reviewed by Australian Stem Cell Registry —
LEIi020-A 1049ips2 McLenachan Lions Eye Institute fibroblast — usher syndrome type 1b False Not yet reviewed by Australian Stem Cell Registry —
LEIi020-B 1049ips9 McLenachan Lions Eye Institute fibroblast — usher syndrome type 1b False Not yet reviewed by Australian Stem Cell Registry —