ProfileGDS1065 / 212228_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 96% 95% 97% 96% 95% 95% 97% 95% 96% 94% 94% 96% 96% 97% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11286.496
GSM24653Normal subject 2913.195
GSM24654Normal subject 32473.997
GSM24655A3243G-MELAS subject 1729.596
GSM24656A3243G-MELAS subject 2920.695
GSM24657A3243G-MELAS subject 31355.295
GSM24658A3243G-MELAS subject 41410.797
GSM24659A3243G-PEO subject 1570.395
GSM24660A3243G-PEO subject 2962.396
GSM24661A3243G-PEO subject 3525.894
GSM24662A3243G-PEO subject 4609.294
GSM24663mtDNA "Common"-deletion subject 11248.796
GSM24664mtDNA "Common"-deletion subject 21938.496
GSM24665mtDNA "Common"-deletion subject 32554.697
GSM24666mtDNA "Common"-deletion subject 41596.795