ProfileGDS1065 / 214666_x_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 0% 22% 31% 2% 26% 22% 2% 20% 25% 7% 5% 24% 22% 30% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 10.20
GSM24653Normal subject 210.222
GSM24654Normal subject 321.631
GSM24655A3243G-MELAS subject 11.42
GSM24656A3243G-MELAS subject 215.526
GSM24657A3243G-MELAS subject 313.522
GSM24658A3243G-MELAS subject 41.32
GSM24659A3243G-PEO subject 18.620
GSM24660A3243G-PEO subject 212.525
GSM24661A3243G-PEO subject 32.37
GSM24662A3243G-PEO subject 42.35
GSM24663mtDNA "Common"-deletion subject 111.824
GSM24664mtDNA "Common"-deletion subject 219.322
GSM24665mtDNA "Common"-deletion subject 325.530
GSM24666mtDNA "Common"-deletion subject 418.825