ProfileGDS1065 / 212464_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 89% 92% 94% 92% 79% 90% 91% 88% 86% 91% 88% 90% 80% 88% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1372.389
GSM24653Normal subject 2516.992
GSM24654Normal subject 3936.894
GSM24655A3243G-MELAS subject 1305.992
GSM24656A3243G-MELAS subject 2167.379
GSM24657A3243G-MELAS subject 3633.590
GSM24658A3243G-MELAS subject 4449.191
GSM24659A3243G-PEO subject 1229.388
GSM24660A3243G-PEO subject 2239.786
GSM24661A3243G-PEO subject 3329.791
GSM24662A3243G-PEO subject 4277.388
GSM24663mtDNA "Common"-deletion subject 1447.690
GSM24664mtDNA "Common"-deletion subject 2328.480
GSM24665mtDNA "Common"-deletion subject 355688
GSM24666mtDNA "Common"-deletion subject 462588