ProfileGDS1065 / 215157_x_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 85% 86% 91% 92% 87% 86% 94% 84% 84% 76% 79% 84% 92% 90% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1275.185
GSM24653Normal subject 2249.986
GSM24654Normal subject 3614.791
GSM24655A3243G-MELAS subject 130392
GSM24656A3243G-MELAS subject 2303.487
GSM24657A3243G-MELAS subject 3437.586
GSM24658A3243G-MELAS subject 4700.794
GSM24659A3243G-PEO subject 1163.284
GSM24660A3243G-PEO subject 2205.284
GSM24661A3243G-PEO subject 394.976
GSM24662A3243G-PEO subject 4139.579
GSM24663mtDNA "Common"-deletion subject 1243.584
GSM24664mtDNA "Common"-deletion subject 287092
GSM24665mtDNA "Common"-deletion subject 3686.290
GSM24666mtDNA "Common"-deletion subject 4512.786