ProfileGDS1065 / 206738_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% 70% 59% 67% 66% 55% 63% 70% 60% 59% 57% 55% 56% 53% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 163.659
GSM24653Normal subject 2100.770
GSM24654Normal subject 379.659
GSM24655A3243G-MELAS subject 16067
GSM24656A3243G-MELAS subject 285.966
GSM24657A3243G-MELAS subject 381.655
GSM24658A3243G-MELAS subject 470.163
GSM24659A3243G-PEO subject 178.370
GSM24660A3243G-PEO subject 261.160
GSM24661A3243G-PEO subject 344.659
GSM24662A3243G-PEO subject 44957
GSM24663mtDNA "Common"-deletion subject 155.555
GSM24664mtDNA "Common"-deletion subject 299.656
GSM24665mtDNA "Common"-deletion subject 375.453
GSM24666mtDNA "Common"-deletion subject 473.252