ProfileGDS1065 / 218949_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 80% 69% 87% 81% 81% 74% 82% 79% 72% 74% 71% 79% 79% 85% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1179.880
GSM24653Normal subject 294.869
GSM24654Normal subject 3383.487
GSM24655A3243G-MELAS subject 1116.981
GSM24656A3243G-MELAS subject 2187.881
GSM24657A3243G-MELAS subject 3196.874
GSM24658A3243G-MELAS subject 4187.282
GSM24659A3243G-PEO subject 1124.779
GSM24660A3243G-PEO subject 2101.872
GSM24661A3243G-PEO subject 385.174
GSM24662A3243G-PEO subject 488.571
GSM24663mtDNA "Common"-deletion subject 117479
GSM24664mtDNA "Common"-deletion subject 2297.279
GSM24665mtDNA "Common"-deletion subject 3397.985
GSM24666mtDNA "Common"-deletion subject 4295.779