ProfileGDS1065 / 220645_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 7% 7% 9% 10% 10% 10% 7% 10% 10% 19% 21% 11% 6% 9% 9% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.27
GSM24653Normal subject 23.37
GSM24654Normal subject 34.39
GSM24655A3243G-MELAS subject 13.610
GSM24656A3243G-MELAS subject 24.910
GSM24657A3243G-MELAS subject 35.310
GSM24658A3243G-MELAS subject 42.47
GSM24659A3243G-PEO subject 14.510
GSM24660A3243G-PEO subject 24.410
GSM24661A3243G-PEO subject 36.219
GSM24662A3243G-PEO subject 48.421
GSM24663mtDNA "Common"-deletion subject 14.711
GSM24664mtDNA "Common"-deletion subject 25.16
GSM24665mtDNA "Common"-deletion subject 35.39
GSM24666mtDNA "Common"-deletion subject 45.19