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	Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Not yet reviewed by Australian Stem Cell Registry	—
HPIi001-B	iPS-6303-R12	Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Not yet reviewed by Australian Stem Cell Registry	—
HPIi002-A	iPS-789-C1	Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Not yet reviewed by Australian Stem Cell Registry	—
HPIi002-B	iPS-789-C2	Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Not yet reviewed by Australian Stem Cell Registry	—
HPIi003-A	iPS-7247-C5	Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Not yet reviewed by Australian Stem Cell Registry	—
HPIi004-A	iPS-5964-R3	Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Not yet reviewed by Australian Stem Cell Registry	—
HPIi004-B	iPS-5964-R6	Clayton	Harry Perkins Institute of Medical Research	LCL	—	congenital myopathy 2a, typical, autosomal dominant	False	Not yet reviewed by Australian Stem Cell Registry	—