ProfileGDS1065 / 210955_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 24% 28% 21% 69% 22% 22% 29% 28% 24% 24% 46% 52% 17% 15% 18% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 111.624
GSM24653Normal subject 215.128
GSM24654Normal subject 310.721
GSM24655A3243G-MELAS subject 165.969
GSM24656A3243G-MELAS subject 21222
GSM24657A3243G-MELAS subject 313.422
GSM24658A3243G-MELAS subject 413.629
GSM24659A3243G-PEO subject 114.328
GSM24660A3243G-PEO subject 211.624
GSM24661A3243G-PEO subject 38.124
GSM24662A3243G-PEO subject 432.346
GSM24663mtDNA "Common"-deletion subject 148.552
GSM24664mtDNA "Common"-deletion subject 212.717
GSM24665mtDNA "Common"-deletion subject 38.615
GSM24666mtDNA "Common"-deletion subject 410.418