ProfileGDS1065 / 202395_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% 88% 83% 79% 80% 81% 80% 85% 79% 81% 81% 86% 85% 75% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1386.989
GSM24653Normal subject 2303.688
GSM24654Normal subject 3290.683
GSM24655A3243G-MELAS subject 1107.479
GSM24656A3243G-MELAS subject 2176.480
GSM24657A3243G-MELAS subject 3315.981
GSM24658A3243G-MELAS subject 4173.380
GSM24659A3243G-PEO subject 1173.685
GSM24660A3243G-PEO subject 2144.879
GSM24661A3243G-PEO subject 313281
GSM24662A3243G-PEO subject 4157.481
GSM24663mtDNA "Common"-deletion subject 1285.286
GSM24664mtDNA "Common"-deletion subject 245285
GSM24665mtDNA "Common"-deletion subject 3211.575
GSM24666mtDNA "Common"-deletion subject 437182