ProfileGDS1065 / 209182_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 51% 47% 43% 43% 42% 56% 43% 69% 50% 51% 53% 47% 47% 32% 39% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14651
GSM24653Normal subject 237.447
GSM24654Normal subject 338.543
GSM24655A3243G-MELAS subject 12543
GSM24656A3243G-MELAS subject 233.842
GSM24657A3243G-MELAS subject 383.956
GSM24658A3243G-MELAS subject 428.843
GSM24659A3243G-PEO subject 177.769
GSM24660A3243G-PEO subject 241.650
GSM24661A3243G-PEO subject 332.851
GSM24662A3243G-PEO subject 44253
GSM24663mtDNA "Common"-deletion subject 139.847
GSM24664mtDNA "Common"-deletion subject 271.647
GSM24665mtDNA "Common"-deletion subject 328.632
GSM24666mtDNA "Common"-deletion subject 440.539