ProfileGDS1065 / 222111_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 60% 47% 58% 63% 71% 43% 62% 52% 60% 60% 45% 12% 63% 59% 57% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 166.260
GSM24653Normal subject 237.747
GSM24654Normal subject 374.958
GSM24655A3243G-MELAS subject 152.963
GSM24656A3243G-MELAS subject 2111.871
GSM24657A3243G-MELAS subject 348.143
GSM24658A3243G-MELAS subject 466.762
GSM24659A3243G-PEO subject 140.252
GSM24660A3243G-PEO subject 260.760
GSM24661A3243G-PEO subject 346.260
GSM24662A3243G-PEO subject 430.745
GSM24663mtDNA "Common"-deletion subject 14.912
GSM24664mtDNA "Common"-deletion subject 2133.563
GSM24665mtDNA "Common"-deletion subject 393.159
GSM24666mtDNA "Common"-deletion subject 491.157