ProfileGDS1065 / 204350_s_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 70% 74% 78% 59% 63% 72% 72% 66% 67% 65% 65% 71% 67% 81% 77% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1105.670
GSM24653Normal subject 2120.174
GSM24654Normal subject 3200.778
GSM24655A3243G-MELAS subject 144.259
GSM24656A3243G-MELAS subject 27763
GSM24657A3243G-MELAS subject 3183.972
GSM24658A3243G-MELAS subject 4109.772
GSM24659A3243G-PEO subject 167.666
GSM24660A3243G-PEO subject 28267
GSM24661A3243G-PEO subject 357.765
GSM24662A3243G-PEO subject 469.165
GSM24663mtDNA "Common"-deletion subject 1115.971
GSM24664mtDNA "Common"-deletion subject 2160.567
GSM24665mtDNA "Common"-deletion subject 3292.281
GSM24666mtDNA "Common"-deletion subject 4256.377