ProfileGDS1065 / 217124_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 50% 57% 47% 47% 50% 52% 45% 51% 43% 52% 51% 55% 46% 53% 44% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 143.950
GSM24653Normal subject 255.757
GSM24654Normal subject 346.547
GSM24655A3243G-MELAS subject 128.747
GSM24656A3243G-MELAS subject 246.850
GSM24657A3243G-MELAS subject 369.152
GSM24658A3243G-MELAS subject 431.445
GSM24659A3243G-PEO subject 139.551
GSM24660A3243G-PEO subject 230.743
GSM24661A3243G-PEO subject 333.952
GSM24662A3243G-PEO subject 439.151
GSM24663mtDNA "Common"-deletion subject 155.855
GSM24664mtDNA "Common"-deletion subject 266.646
GSM24665mtDNA "Common"-deletion subject 372.553
GSM24666mtDNA "Common"-deletion subject 451.544