ProfileGDS1065 / 202231_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 92% 93% 92% 94% 93% 95% 93% 94% 94% 94% 94% 95% 95% 92% 94% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1529.292
GSM24653Normal subject 254893
GSM24654Normal subject 3668.392
GSM24655A3243G-MELAS subject 1424.294
GSM24656A3243G-MELAS subject 2556.693
GSM24657A3243G-MELAS subject 31409.495
GSM24658A3243G-MELAS subject 4589.493
GSM24659A3243G-PEO subject 1532.294
GSM24660A3243G-PEO subject 2582.794
GSM24661A3243G-PEO subject 3510.594
GSM24662A3243G-PEO subject 4658.494
GSM24663mtDNA "Common"-deletion subject 1863.695
GSM24664mtDNA "Common"-deletion subject 21517.695
GSM24665mtDNA "Common"-deletion subject 3868.492
GSM24666mtDNA "Common"-deletion subject 41255.794