ProfileGDS1065 / 204234_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 43% 46% 66% 57% 54% 43% 48% 36% 38% 46% 42% 60% 57% 57% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 132.743
GSM24653Normal subject 236.746
GSM24654Normal subject 3106.866
GSM24655A3243G-MELAS subject 141.157
GSM24656A3243G-MELAS subject 255.354
GSM24657A3243G-MELAS subject 346.943
GSM24658A3243G-MELAS subject 436.948
GSM24659A3243G-PEO subject 121.536
GSM24660A3243G-PEO subject 224.938
GSM24661A3243G-PEO subject 326.746
GSM24662A3243G-PEO subject 42742
GSM24663mtDNA "Common"-deletion subject 167.960
GSM24664mtDNA "Common"-deletion subject 2103.557
GSM24665mtDNA "Common"-deletion subject 388.357
GSM24666mtDNA "Common"-deletion subject 484.556