ProfileGDS1065 / 212976_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 19% 5% 18% 1% 13% 26% 26% 4% 16% 19% 20% 7% 12% 7% 35% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.719
GSM24653Normal subject 22.75
GSM24654Normal subject 38.518
GSM24655A3243G-MELAS subject 111
GSM24656A3243G-MELAS subject 2613
GSM24657A3243G-MELAS subject 318.526
GSM24658A3243G-MELAS subject 411.426
GSM24659A3243G-PEO subject 12.34
GSM24660A3243G-PEO subject 26.716
GSM24661A3243G-PEO subject 36.219
GSM24662A3243G-PEO subject 47.720
GSM24663mtDNA "Common"-deletion subject 13.27
GSM24664mtDNA "Common"-deletion subject 2912
GSM24665mtDNA "Common"-deletion subject 34.37
GSM24666mtDNA "Common"-deletion subject 432.835