ProfileGDS1065 / 220189_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 55% 57% 57% 61% 63% 62% 57% 53% 64% 51% 62% 61% 56% 62% 48% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 154.655
GSM24653Normal subject 25657
GSM24654Normal subject 370.557
GSM24655A3243G-MELAS subject 148.461
GSM24656A3243G-MELAS subject 279.463
GSM24657A3243G-MELAS subject 3109.762
GSM24658A3243G-MELAS subject 452.457
GSM24659A3243G-PEO subject 141.353
GSM24660A3243G-PEO subject 270.964
GSM24661A3243G-PEO subject 332.551
GSM24662A3243G-PEO subject 46062
GSM24663mtDNA "Common"-deletion subject 173.261
GSM24664mtDNA "Common"-deletion subject 2101.656
GSM24665mtDNA "Common"-deletion subject 3106.262
GSM24666mtDNA "Common"-deletion subject 461.148