ProfileGDS1065 / 210031_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 46% 41% 41% 56% 45% 55% 59% 55% 49% 55% 56% 46% 54% 53% 49% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 137.446
GSM24653Normal subject 228.741
GSM24654Normal subject 335.241
GSM24655A3243G-MELAS subject 140.256
GSM24656A3243G-MELAS subject 239.445
GSM24657A3243G-MELAS subject 38155
GSM24658A3243G-MELAS subject 45859
GSM24659A3243G-PEO subject 145.655
GSM24660A3243G-PEO subject 239.449
GSM24661A3243G-PEO subject 338.555
GSM24662A3243G-PEO subject 447.156
GSM24663mtDNA "Common"-deletion subject 138.946
GSM24664mtDNA "Common"-deletion subject 292.554
GSM24665mtDNA "Common"-deletion subject 372.753
GSM24666mtDNA "Common"-deletion subject 463.349