ProfileGDS1065 / 212882_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 69% 68% 69% 75% 64% 64% 68% 70% 64% 63% 63% 76% 65% 67% 63% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 199.569
GSM24653Normal subject 288.668
GSM24654Normal subject 3126.169
GSM24655A3243G-MELAS subject 18575
GSM24656A3243G-MELAS subject 280.564
GSM24657A3243G-MELAS subject 312064
GSM24658A3243G-MELAS subject 488.968
GSM24659A3243G-PEO subject 180.970
GSM24660A3243G-PEO subject 271.164
GSM24661A3243G-PEO subject 354.163
GSM24662A3243G-PEO subject 463.563
GSM24663mtDNA "Common"-deletion subject 1144.176
GSM24664mtDNA "Common"-deletion subject 214965
GSM24665mtDNA "Common"-deletion subject 3135.467
GSM24666mtDNA "Common"-deletion subject 4121.163