ProfileGDS1065 / 216592_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 19% 12% 25% 34% 40% 15% 15% 41% 31% 11% 28% 15% 42% 32% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.219
GSM24653Normal subject 24.812
GSM24654Normal subject 314.425
GSM24655A3243G-MELAS subject 116.334
GSM24656A3243G-MELAS subject 232.140
GSM24657A3243G-MELAS subject 37.915
GSM24658A3243G-MELAS subject 44.915
GSM24659A3243G-PEO subject 126.341
GSM24660A3243G-PEO subject 21731
GSM24661A3243G-PEO subject 33.411
GSM24662A3243G-PEO subject 413.628
GSM24663mtDNA "Common"-deletion subject 16.215
GSM24664mtDNA "Common"-deletion subject 255.942
GSM24665mtDNA "Common"-deletion subject 329.132
GSM24666mtDNA "Common"-deletion subject 427.131