ProfileGDS1065 / 221357_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 73% 27% 63% 26% 71% 60% 72% 23% 58% 46% 40% 28% 26% 71% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1120.373
GSM24653Normal subject 213.527
GSM24654Normal subject 395.663
GSM24655A3243G-MELAS subject 110.426
GSM24656A3243G-MELAS subject 2109.471
GSM24657A3243G-MELAS subject 3100.360
GSM24658A3243G-MELAS subject 410772
GSM24659A3243G-PEO subject 110.823
GSM24660A3243G-PEO subject 257.258
GSM24661A3243G-PEO subject 326.746
GSM24662A3243G-PEO subject 424.940
GSM24663mtDNA "Common"-deletion subject 114.728
GSM24664mtDNA "Common"-deletion subject 224.526
GSM24665mtDNA "Common"-deletion subject 3161.871
GSM24666mtDNA "Common"-deletion subject 426.931