ProfileGDS1065 / 206838_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 14% 9% 25% 10% 18% 26% 14% 8% 16% 8% 22% 24% 28% 24% 29% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15.714
GSM24653Normal subject 23.99
GSM24654Normal subject 314.225
GSM24655A3243G-MELAS subject 13.610
GSM24656A3243G-MELAS subject 28.918
GSM24657A3243G-MELAS subject 318.526
GSM24658A3243G-MELAS subject 44.614
GSM24659A3243G-PEO subject 13.88
GSM24660A3243G-PEO subject 26.916
GSM24661A3243G-PEO subject 32.78
GSM24662A3243G-PEO subject 48.622
GSM24663mtDNA "Common"-deletion subject 111.624
GSM24664mtDNA "Common"-deletion subject 228.528
GSM24665mtDNA "Common"-deletion subject 316.624
GSM24666mtDNA "Common"-deletion subject 423.529