ProfileGDS1065 / 221762_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 79% 74% 73% 47% 78% 72% 73% 79% 81% 80% 80% 79% 68% 73% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1170.179
GSM24653Normal subject 2117.274
GSM24654Normal subject 3149.573
GSM24655A3243G-MELAS subject 128.947
GSM24656A3243G-MELAS subject 2157.478
GSM24657A3243G-MELAS subject 3178.172
GSM24658A3243G-MELAS subject 4112.873
GSM24659A3243G-PEO subject 1121.179
GSM24660A3243G-PEO subject 2167.581
GSM24661A3243G-PEO subject 3120.480
GSM24662A3243G-PEO subject 4146.280
GSM24663mtDNA "Common"-deletion subject 1175.979
GSM24664mtDNA "Common"-deletion subject 2169.768
GSM24665mtDNA "Common"-deletion subject 3181.473
GSM24666mtDNA "Common"-deletion subject 4169.470