ProfileGDS1065 / 209406_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 67% 71% 85% 78% 74% 68% 71% 60% 68% 53% 47% 69% 78% 81% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 191.367
GSM24653Normal subject 2104.971
GSM24654Normal subject 3334.685
GSM24655A3243G-MELAS subject 1103.578
GSM24656A3243G-MELAS subject 2129.274
GSM24657A3243G-MELAS subject 314368
GSM24658A3243G-MELAS subject 4104.171
GSM24659A3243G-PEO subject 154.960
GSM24660A3243G-PEO subject 283.868
GSM24661A3243G-PEO subject 33553
GSM24662A3243G-PEO subject 43347
GSM24663mtDNA "Common"-deletion subject 1100.969
GSM24664mtDNA "Common"-deletion subject 2277.878
GSM24665mtDNA "Common"-deletion subject 3307.681
GSM24666mtDNA "Common"-deletion subject 4186.271