ProfileGDS1065 / 206328_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 59% 47% 51% 48% 52% 58% 50% 62% 59% 67% 63% 58% 54% 44% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 165.159
GSM24653Normal subject 238.447
GSM24654Normal subject 354.651
GSM24655A3243G-MELAS subject 130.348
GSM24656A3243G-MELAS subject 25152
GSM24657A3243G-MELAS subject 391.158
GSM24658A3243G-MELAS subject 439.850
GSM24659A3243G-PEO subject 158.962
GSM24660A3243G-PEO subject 257.959
GSM24661A3243G-PEO subject 364.267
GSM24662A3243G-PEO subject 464.563
GSM24663mtDNA "Common"-deletion subject 164.758
GSM24664mtDNA "Common"-deletion subject 293.654
GSM24665mtDNA "Common"-deletion subject 349.644
GSM24666mtDNA "Common"-deletion subject 487.956