ProfileGDS1065 / 202519_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 91% 86% 88% 80% 89% 90% 87% 81% 90% 86% 88% 88% 85% 88% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1496.791
GSM24653Normal subject 2253.286
GSM24654Normal subject 3414.888
GSM24655A3243G-MELAS subject 1116.580
GSM24656A3243G-MELAS subject 2335.389
GSM24657A3243G-MELAS subject 3639.690
GSM24658A3243G-MELAS subject 4279.487
GSM24659A3243G-PEO subject 113681
GSM24660A3243G-PEO subject 2372.990
GSM24661A3243G-PEO subject 3188.386
GSM24662A3243G-PEO subject 4273.588
GSM24663mtDNA "Common"-deletion subject 1366.688
GSM24664mtDNA "Common"-deletion subject 2465.585
GSM24665mtDNA "Common"-deletion subject 3554.388
GSM24666mtDNA "Common"-deletion subject 4598.388