ProfileGDS1065 / 210290_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 41% 36% 41% 46% 19% 36% 38% 45% 48% 41% 47% 54% 38% 13% 39% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 130.341
GSM24653Normal subject 222.836
GSM24654Normal subject 33641
GSM24655A3243G-MELAS subject 128.246
GSM24656A3243G-MELAS subject 29.719
GSM24657A3243G-MELAS subject 332.936
GSM24658A3243G-MELAS subject 423.338
GSM24659A3243G-PEO subject 131.145
GSM24660A3243G-PEO subject 23848
GSM24661A3243G-PEO subject 321.341
GSM24662A3243G-PEO subject 433.247
GSM24663mtDNA "Common"-deletion subject 153.654
GSM24664mtDNA "Common"-deletion subject 247.938
GSM24665mtDNA "Common"-deletion subject 37.513
GSM24666mtDNA "Common"-deletion subject 440.239