ProfileGDS1065 / 209447_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 77% 79% 83% 81% 84% 77% 82% 76% 79% 61% 68% 76% 79% 81% 81% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1154.377
GSM24653Normal subject 2161.579
GSM24654Normal subject 3282.183
GSM24655A3243G-MELAS subject 1118.881
GSM24656A3243G-MELAS subject 2225.884
GSM24657A3243G-MELAS subject 3236.577
GSM24658A3243G-MELAS subject 4195.182
GSM24659A3243G-PEO subject 1104.376
GSM24660A3243G-PEO subject 2145.379
GSM24661A3243G-PEO subject 349.161
GSM24662A3243G-PEO subject 479.168
GSM24663mtDNA "Common"-deletion subject 1150.476
GSM24664mtDNA "Common"-deletion subject 230079
GSM24665mtDNA "Common"-deletion subject 329181
GSM24666mtDNA "Common"-deletion subject 4348.581