ProfileGDS1065 / 213802_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 11% 7% 18% 25% 15% 12% 7% 2% 15% 10% 3% 19% 12% 3% 16% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.511
GSM24653Normal subject 23.17
GSM24654Normal subject 38.618
GSM24655A3243G-MELAS subject 19.825
GSM24656A3243G-MELAS subject 27.415
GSM24657A3243G-MELAS subject 36.712
GSM24658A3243G-MELAS subject 42.67
GSM24659A3243G-PEO subject 11.42
GSM24660A3243G-PEO subject 26.415
GSM24661A3243G-PEO subject 33.310
GSM24662A3243G-PEO subject 41.63
GSM24663mtDNA "Common"-deletion subject 18.319
GSM24664mtDNA "Common"-deletion subject 28.712
GSM24665mtDNA "Common"-deletion subject 32.73
GSM24666mtDNA "Common"-deletion subject 49.316