ProfileGDS1065 / 220341_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 47% 25% 24% 19% 41% 49% 44% 25% 42% 21% 25% 55% 41% 43% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 139.747
GSM24653Normal subject 212.225
GSM24654Normal subject 313.424
GSM24655A3243G-MELAS subject 16.619
GSM24656A3243G-MELAS subject 232.441
GSM24657A3243G-MELAS subject 361.249
GSM24658A3243G-MELAS subject 43044
GSM24659A3243G-PEO subject 111.925
GSM24660A3243G-PEO subject 230.442
GSM24661A3243G-PEO subject 36.821
GSM24662A3243G-PEO subject 410.825
GSM24663mtDNA "Common"-deletion subject 155.555
GSM24664mtDNA "Common"-deletion subject 255.341
GSM24665mtDNA "Common"-deletion subject 347.543
GSM24666mtDNA "Common"-deletion subject 486.156