ProfileGDS1065 / 213923_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 62% 73% 61% 78% 65% 65% 63% 71% 61% 65% 65% 70% 69% 57% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 172.262
GSM24653Normal subject 2115.173
GSM24654Normal subject 387.161
GSM24655A3243G-MELAS subject 1100.778
GSM24656A3243G-MELAS subject 285.665
GSM24657A3243G-MELAS subject 3124.465
GSM24658A3243G-MELAS subject 468.763
GSM24659A3243G-PEO subject 183.571
GSM24660A3243G-PEO subject 262.961
GSM24661A3243G-PEO subject 358.565
GSM24662A3243G-PEO subject 469.365
GSM24663mtDNA "Common"-deletion subject 1109.670
GSM24664mtDNA "Common"-deletion subject 2176.969
GSM24665mtDNA "Common"-deletion subject 38657
GSM24666mtDNA "Common"-deletion subject 413665