ProfileGDS1065 / 209627_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% 74% 51% 44% 46% 48% 57% 63% 61% 60% 46% 51% 73% 54% 69% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 154.355
GSM24653Normal subject 2121.674
GSM24654Normal subject 355.251
GSM24655A3243G-MELAS subject 125.544
GSM24656A3243G-MELAS subject 240.346
GSM24657A3243G-MELAS subject 359.148
GSM24658A3243G-MELAS subject 453.257
GSM24659A3243G-PEO subject 161.763
GSM24660A3243G-PEO subject 263.461
GSM24661A3243G-PEO subject 346.860
GSM24662A3243G-PEO subject 431.546
GSM24663mtDNA "Common"-deletion subject 146.951
GSM24664mtDNA "Common"-deletion subject 2211.973
GSM24665mtDNA "Common"-deletion subject 378.754
GSM24666mtDNA "Common"-deletion subject 4167.569