ProfileGDS1065 / 208005_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 6% 9% 27% 17% 17% 27% 6% 39% 18% 31% 19% 19% 15% 31% 13% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 136
GSM24653Normal subject 23.89
GSM24654Normal subject 315.927
GSM24655A3243G-MELAS subject 16.117
GSM24656A3243G-MELAS subject 2817
GSM24657A3243G-MELAS subject 319.427
GSM24658A3243G-MELAS subject 42.36
GSM24659A3243G-PEO subject 124.439
GSM24660A3243G-PEO subject 27.618
GSM24661A3243G-PEO subject 31331
GSM24662A3243G-PEO subject 4719
GSM24663mtDNA "Common"-deletion subject 1819
GSM24664mtDNA "Common"-deletion subject 210.815
GSM24665mtDNA "Common"-deletion subject 326.731
GSM24666mtDNA "Common"-deletion subject 46.913