ProfileGDS1065 / 221300_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 59% 64% 61% 63% 62% 50% 58% 67% 68% 65% 65% 67% 61% 63% 57% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 163.659
GSM24653Normal subject 275.864
GSM24654Normal subject 383.961
GSM24655A3243G-MELAS subject 152.463
GSM24656A3243G-MELAS subject 27662
GSM24657A3243G-MELAS subject 363.450
GSM24658A3243G-MELAS subject 45658
GSM24659A3243G-PEO subject 170.267
GSM24660A3243G-PEO subject 284.568
GSM24661A3243G-PEO subject 356.465
GSM24662A3243G-PEO subject 469.965
GSM24663mtDNA "Common"-deletion subject 194.167
GSM24664mtDNA "Common"-deletion subject 2124.561
GSM24665mtDNA "Common"-deletion subject 3112.763
GSM24666mtDNA "Common"-deletion subject 490.357