ProfileGDS1065 / 207289_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% 35% 49% 62% 45% 44% 49% 67% 46% 47% 54% 28% 51% 42% 45% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 160.558
GSM24653Normal subject 222.135
GSM24654Normal subject 350.649
GSM24655A3243G-MELAS subject 149.862
GSM24656A3243G-MELAS subject 238.245
GSM24657A3243G-MELAS subject 350.244
GSM24658A3243G-MELAS subject 437.949
GSM24659A3243G-PEO subject 170.967
GSM24660A3243G-PEO subject 23546
GSM24661A3243G-PEO subject 327.447
GSM24662A3243G-PEO subject 444.854
GSM24663mtDNA "Common"-deletion subject 114.628
GSM24664mtDNA "Common"-deletion subject 282.651
GSM24665mtDNA "Common"-deletion subject 347.142
GSM24666mtDNA "Common"-deletion subject 454.545