ProfileGDS1065 / 221919_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 42% 28% 40% 30% 41% 41% 45% 27% 31% 31% 25% 47% 47% 39% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 132.542
GSM24653Normal subject 214.928
GSM24654Normal subject 333.140
GSM24655A3243G-MELAS subject 113.730
GSM24656A3243G-MELAS subject 233.641
GSM24657A3243G-MELAS subject 342.741
GSM24658A3243G-MELAS subject 432.445
GSM24659A3243G-PEO subject 113.527
GSM24660A3243G-PEO subject 21731
GSM24661A3243G-PEO subject 312.731
GSM24662A3243G-PEO subject 411.125
GSM24663mtDNA "Common"-deletion subject 139.447
GSM24664mtDNA "Common"-deletion subject 269.547
GSM24665mtDNA "Common"-deletion subject 341.239
GSM24666mtDNA "Common"-deletion subject 486.756