ProfileGDS1065 / 217227_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 46% 16% 40% 49% 48% 53% 36% 69% 55% 41% 49% 37% 53% 47% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 137.746
GSM24653Normal subject 26.516
GSM24654Normal subject 33440
GSM24655A3243G-MELAS subject 130.949
GSM24656A3243G-MELAS subject 24348
GSM24657A3243G-MELAS subject 374.153
GSM24658A3243G-MELAS subject 421.336
GSM24659A3243G-PEO subject 176.769
GSM24660A3243G-PEO subject 250.355
GSM24661A3243G-PEO subject 32141
GSM24662A3243G-PEO subject 435.549
GSM24663mtDNA "Common"-deletion subject 125.237
GSM24664mtDNA "Common"-deletion subject 288.753
GSM24665mtDNA "Common"-deletion subject 358.347
GSM24666mtDNA "Common"-deletion subject 42731