ProfileGDS1065 / 218915_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 82% 79% 79% 76% 78% 79% 79% 79% 83% 80% 85% 84% 72% 77% 76% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1205.282
GSM24653Normal subject 2161.379
GSM24654Normal subject 3214.979
GSM24655A3243G-MELAS subject 189.876
GSM24656A3243G-MELAS subject 2157.378
GSM24657A3243G-MELAS subject 3264.879
GSM24658A3243G-MELAS subject 4158.379
GSM24659A3243G-PEO subject 1124.279
GSM24660A3243G-PEO subject 2190.283
GSM24661A3243G-PEO subject 3127.180
GSM24662A3243G-PEO subject 4211.185
GSM24663mtDNA "Common"-deletion subject 124584
GSM24664mtDNA "Common"-deletion subject 2203.272
GSM24665mtDNA "Common"-deletion subject 3235.677
GSM24666mtDNA "Common"-deletion subject 4239.476