ProfileGDS1065 / 203634_s_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 21% 33% 25% 21% 28% 25% 20% 18% 27% 19% 22% 29% 25% 26% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.421
GSM24653Normal subject 220.333
GSM24654Normal subject 313.625
GSM24655A3243G-MELAS subject 17.521
GSM24656A3243G-MELAS subject 21728
GSM24657A3243G-MELAS subject 317.925
GSM24658A3243G-MELAS subject 47.220
GSM24659A3243G-PEO subject 17.418
GSM24660A3243G-PEO subject 213.727
GSM24661A3243G-PEO subject 35.919
GSM24662A3243G-PEO subject 48.622
GSM24663mtDNA "Common"-deletion subject 11629
GSM24664mtDNA "Common"-deletion subject 222.925
GSM24665mtDNA "Common"-deletion subject 319.926
GSM24666mtDNA "Common"-deletion subject 418.825