Cell Line Identifier	Alternative Names	Maintainer	Producer	Parental Cell Type	Tissue of Origin	Disease as reported	Modified?	Curation Status	Related Lines
HPIi001-A	iPS-6303-C6B3	Joshua Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Reviewed by Australian Stem Cell Registry	—
HPIi001-B	iPS-6303-R12	Joshua Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Reviewed by Australian Stem Cell Registry	—
HPIi002-A	iPS-789-C1	Joshua Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Reviewed by Australian Stem Cell Registry	—
HPIi002-B	iPS-789-C2	Joshua Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Reviewed by Australian Stem Cell Registry	—
HPIi003-A	iPS-7247-C5	Joshua Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Reviewed by Australian Stem Cell Registry	—
HPIi004-A	iPS-5964-R3	Joshua Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Reviewed by Australian Stem Cell Registry	—
HPIi004-B	iPS-5964-R6	Joshua Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Reviewed by Australian Stem Cell Registry	—