ProfileGDS1065 / 205748_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 60% 54% 65% 46% 62% 61% 59% 57% 65% 69% 57% 58% 66% 58% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 167.960
GSM24653Normal subject 250.154
GSM24654Normal subject 3104.565
GSM24655A3243G-MELAS subject 127.646
GSM24656A3243G-MELAS subject 275.762
GSM24657A3243G-MELAS subject 3104.661
GSM24658A3243G-MELAS subject 457.459
GSM24659A3243G-PEO subject 148.757
GSM24660A3243G-PEO subject 275.465
GSM24661A3243G-PEO subject 36869
GSM24662A3243G-PEO subject 449.157
GSM24663mtDNA "Common"-deletion subject 162.958
GSM24664mtDNA "Common"-deletion subject 2155.466
GSM24665mtDNA "Common"-deletion subject 38958
GSM24666mtDNA "Common"-deletion subject 4134.265