ProfileGDS1065 / 218302_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 37% 29% 62% 52% 46% 50% 57% 52% 54% 42% 42% 40% 55% 47% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 124.937
GSM24653Normal subject 216.229
GSM24654Normal subject 38962
GSM24655A3243G-MELAS subject 135.152
GSM24656A3243G-MELAS subject 240.946
GSM24657A3243G-MELAS subject 362.950
GSM24658A3243G-MELAS subject 452.157
GSM24659A3243G-PEO subject 140.452
GSM24660A3243G-PEO subject 247.854
GSM24661A3243G-PEO subject 321.942
GSM24662A3243G-PEO subject 427.642
GSM24663mtDNA "Common"-deletion subject 129.440
GSM24664mtDNA "Common"-deletion subject 294.255
GSM24665mtDNA "Common"-deletion subject 356.647
GSM24666mtDNA "Common"-deletion subject 439.138