ProfileGDS1065 / 203757_s_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 51% 47% 43% 54% 56% 30% 44% 44% 54% 52% 31% 49% 50% 47% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 145.351
GSM24653Normal subject 237.347
GSM24654Normal subject 339.443
GSM24655A3243G-MELAS subject 137.954
GSM24656A3243G-MELAS subject 259.756
GSM24657A3243G-MELAS subject 323.630
GSM24658A3243G-MELAS subject 430.344
GSM24659A3243G-PEO subject 130.244
GSM24660A3243G-PEO subject 248.654
GSM24661A3243G-PEO subject 333.952
GSM24662A3243G-PEO subject 416.331
GSM24663mtDNA "Common"-deletion subject 143.549
GSM24664mtDNA "Common"-deletion subject 28050
GSM24665mtDNA "Common"-deletion subject 357.847
GSM24666mtDNA "Common"-deletion subject 430.133