ProfileGDS1065 / 206110_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 3% 28% 13% 4% 5% 15% 12% 25% 13% 19% 34% 29% 31% 11% 11% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 123
GSM24653Normal subject 214.928
GSM24654Normal subject 35.913
GSM24655A3243G-MELAS subject 124
GSM24656A3243G-MELAS subject 23.25
GSM24657A3243G-MELAS subject 38.115
GSM24658A3243G-MELAS subject 44.212
GSM24659A3243G-PEO subject 111.925
GSM24660A3243G-PEO subject 25.513
GSM24661A3243G-PEO subject 35.819
GSM24662A3243G-PEO subject 419.234
GSM24663mtDNA "Common"-deletion subject 116.329
GSM24664mtDNA "Common"-deletion subject 234.331
GSM24665mtDNA "Common"-deletion subject 36.611
GSM24666mtDNA "Common"-deletion subject 46.211