ProfileGDS1065 / 220534_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 44% 30% 32% 55% 41% 31% 27% 55% 43% 43% 52% 38% 39% 41% 19% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 135.244
GSM24653Normal subject 216.830
GSM24654Normal subject 321.832
GSM24655A3243G-MELAS subject 139.155
GSM24656A3243G-MELAS subject 232.441
GSM24657A3243G-MELAS subject 325.631
GSM24658A3243G-MELAS subject 412.227
GSM24659A3243G-PEO subject 144.755
GSM24660A3243G-PEO subject 231.643
GSM24661A3243G-PEO subject 32343
GSM24662A3243G-PEO subject 440.952
GSM24663mtDNA "Common"-deletion subject 126.538
GSM24664mtDNA "Common"-deletion subject 249.639
GSM24665mtDNA "Common"-deletion subject 34441
GSM24666mtDNA "Common"-deletion subject 411.219