ProfileGDS1065 / 200016_x_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 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% 99% 98% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12970.998
GSM24653Normal subject 23303.498
GSM24654Normal subject 33753.798
GSM24655A3243G-MELAS subject 11797.598
GSM24656A3243G-MELAS subject 22948.298
GSM24657A3243G-MELAS subject 34932.598
GSM24658A3243G-MELAS subject 43307.598
GSM24659A3243G-PEO subject 12590.498
GSM24660A3243G-PEO subject 22734.198
GSM24661A3243G-PEO subject 32111.198
GSM24662A3243G-PEO subject 43215.798
GSM24663mtDNA "Common"-deletion subject 13766.498
GSM24664mtDNA "Common"-deletion subject 25857.999
GSM24665mtDNA "Common"-deletion subject 35554.398
GSM24666mtDNA "Common"-deletion subject 45367.198