ProfileGDS1065 / 202625_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 40% 29% 32% 43% 30% 35% 46% 29% 24% 22% 30% 33% 37% 32% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 128.640
GSM24653Normal subject 216.429
GSM24654Normal subject 322.832
GSM24655A3243G-MELAS subject 12543
GSM24656A3243G-MELAS subject 21930
GSM24657A3243G-MELAS subject 331.435
GSM24658A3243G-MELAS subject 433.346
GSM24659A3243G-PEO subject 11529
GSM24660A3243G-PEO subject 211.524
GSM24661A3243G-PEO subject 37.422
GSM24662A3243G-PEO subject 414.630
GSM24663mtDNA "Common"-deletion subject 120.633
GSM24664mtDNA "Common"-deletion subject 246.537
GSM24665mtDNA "Common"-deletion subject 328.932
GSM24666mtDNA "Common"-deletion subject 430.533