ProfileGDS1065 / 219226_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 33% 40% 44% 47% 53% 37% 16% 36% 56% 32% 39% 26% 49% 35% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 120.133
GSM24653Normal subject 227.540
GSM24654Normal subject 340.244
GSM24655A3243G-MELAS subject 128.647
GSM24656A3243G-MELAS subject 252.453
GSM24657A3243G-MELAS subject 334.837
GSM24658A3243G-MELAS subject 45.516
GSM24659A3243G-PEO subject 121.136
GSM24660A3243G-PEO subject 252.156
GSM24661A3243G-PEO subject 313.732
GSM24662A3243G-PEO subject 424.439
GSM24663mtDNA "Common"-deletion subject 112.726
GSM24664mtDNA "Common"-deletion subject 276.349
GSM24665mtDNA "Common"-deletion subject 333.235
GSM24666mtDNA "Common"-deletion subject 426.531