ProfileGDS1065 / 219356_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 81% 77% 82% 84% 83% 81% 82% 71% 78% 74% 76% 77% 85% 85% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1198.281
GSM24653Normal subject 2142.977
GSM24654Normal subject 3264.182
GSM24655A3243G-MELAS subject 114284
GSM24656A3243G-MELAS subject 221683
GSM24657A3243G-MELAS subject 3298.881
GSM24658A3243G-MELAS subject 4199.282
GSM24659A3243G-PEO subject 184.171
GSM24660A3243G-PEO subject 213778
GSM24661A3243G-PEO subject 387.874
GSM24662A3243G-PEO subject 411976
GSM24663mtDNA "Common"-deletion subject 1160.377
GSM24664mtDNA "Common"-deletion subject 2467.985
GSM24665mtDNA "Common"-deletion subject 3408.785
GSM24666mtDNA "Common"-deletion subject 4376.483