ProfileGDS1065 / 214764_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 58% 66% 59% 68% 74% 72% 67% 54% 69% 66% 66% 66% 67% 65% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 162.958
GSM24653Normal subject 280.866
GSM24654Normal subject 378.259
GSM24655A3243G-MELAS subject 162.868
GSM24656A3243G-MELAS subject 2124.474
GSM24657A3243G-MELAS subject 3184.372
GSM24658A3243G-MELAS subject 484.967
GSM24659A3243G-PEO subject 143.254
GSM24660A3243G-PEO subject 289.569
GSM24661A3243G-PEO subject 360.366
GSM24662A3243G-PEO subject 470.766
GSM24663mtDNA "Common"-deletion subject 188.966
GSM24664mtDNA "Common"-deletion subject 2159.167
GSM24665mtDNA "Common"-deletion subject 3122.965
GSM24666mtDNA "Common"-deletion subject 4182.471