ProfileGDS1065 / 213645_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 64% 76% 67% 50% 57% 72% 62% 69% 39% 35% 18% 62% 35% 61% 48% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18164
GSM24653Normal subject 213276
GSM24654Normal subject 3110.267
GSM24655A3243G-MELAS subject 132.750
GSM24656A3243G-MELAS subject 26157
GSM24657A3243G-MELAS subject 3182.272
GSM24658A3243G-MELAS subject 466.662
GSM24659A3243G-PEO subject 177.869
GSM24660A3243G-PEO subject 226.639
GSM24661A3243G-PEO subject 315.935
GSM24662A3243G-PEO subject 46.618
GSM24663mtDNA "Common"-deletion subject 174.762
GSM24664mtDNA "Common"-deletion subject 240.635
GSM24665mtDNA "Common"-deletion subject 3101.561
GSM24666mtDNA "Common"-deletion subject 461.848