ProfileGDS1065 / 209930_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 30% 31% 41% 45% 37% 30% 36% 48% 46% 37% 14% 33% 36% 27% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 116.930
GSM24653Normal subject 218.231
GSM24654Normal subject 335.341
GSM24655A3243G-MELAS subject 126.545
GSM24656A3243G-MELAS subject 227.937
GSM24657A3243G-MELAS subject 323.530
GSM24658A3243G-MELAS subject 420.836
GSM24659A3243G-PEO subject 135.648
GSM24660A3243G-PEO subject 235.846
GSM24661A3243G-PEO subject 317.937
GSM24662A3243G-PEO subject 45.214
GSM24663mtDNA "Common"-deletion subject 120.233
GSM24664mtDNA "Common"-deletion subject 244.536
GSM24665mtDNA "Common"-deletion subject 321.127
GSM24666mtDNA "Common"-deletion subject 43838