ProfileGDS1065 / 221448_s_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 38% 22% 41% 45% 55% 36% 17% 43% 52% 27% 54% 52% 40% 39% 40% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 126.438
GSM24653Normal subject 29.822
GSM24654Normal subject 335.941
GSM24655A3243G-MELAS subject 126.545
GSM24656A3243G-MELAS subject 257.555
GSM24657A3243G-MELAS subject 33436
GSM24658A3243G-MELAS subject 45.917
GSM24659A3243G-PEO subject 129.443
GSM24660A3243G-PEO subject 245.352
GSM24661A3243G-PEO subject 31027
GSM24662A3243G-PEO subject 444.654
GSM24663mtDNA "Common"-deletion subject 149.452
GSM24664mtDNA "Common"-deletion subject 251.640
GSM24665mtDNA "Common"-deletion subject 34039
GSM24666mtDNA "Common"-deletion subject 442.840