ProfileGDS1065 / 214569_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 31% 33% 44% 26% 27% 20% 33% 41% 31% 33% 24% 39% 35% 36% 23% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 118.431
GSM24653Normal subject 220.533
GSM24654Normal subject 340.444
GSM24655A3243G-MELAS subject 110.826
GSM24656A3243G-MELAS subject 216.427
GSM24657A3243G-MELAS subject 312.220
GSM24658A3243G-MELAS subject 417.833
GSM24659A3243G-PEO subject 126.541
GSM24660A3243G-PEO subject 21731
GSM24661A3243G-PEO subject 314.533
GSM24662A3243G-PEO subject 49.924
GSM24663mtDNA "Common"-deletion subject 12839
GSM24664mtDNA "Common"-deletion subject 240.935
GSM24665mtDNA "Common"-deletion subject 334.236
GSM24666mtDNA "Common"-deletion subject 41623