ProfileGDS1065 / 215124_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 48% 25% 32% 47% 43% 34% 41% 42% 43% 33% 41% 39% 42% 37% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 141.348
GSM24653Normal subject 212.425
GSM24654Normal subject 32232
GSM24655A3243G-MELAS subject 128.547
GSM24656A3243G-MELAS subject 236.343
GSM24657A3243G-MELAS subject 331.134
GSM24658A3243G-MELAS subject 426.441
GSM24659A3243G-PEO subject 127.342
GSM24660A3243G-PEO subject 231.543
GSM24661A3243G-PEO subject 313.933
GSM24662A3243G-PEO subject 425.641
GSM24663mtDNA "Common"-deletion subject 128.439
GSM24664mtDNA "Common"-deletion subject 256.842
GSM24665mtDNA "Common"-deletion subject 337.137
GSM24666mtDNA "Common"-deletion subject 417.825