ProfileGDS1065 / 215199_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 34% 25% 19% 37% 11% 45% 29% 35% 19% 26% 40% 47% 11% 24% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 121.534
GSM24653Normal subject 212.525
GSM24654Normal subject 39.419
GSM24655A3243G-MELAS subject 118.837
GSM24656A3243G-MELAS subject 25.411
GSM24657A3243G-MELAS subject 351.445
GSM24658A3243G-MELAS subject 414.229
GSM24659A3243G-PEO subject 12035
GSM24660A3243G-PEO subject 28.419
GSM24661A3243G-PEO subject 39.526
GSM24662A3243G-PEO subject 425.240
GSM24663mtDNA "Common"-deletion subject 139.547
GSM24664mtDNA "Common"-deletion subject 28.311
GSM24665mtDNA "Common"-deletion subject 317.424
GSM24666mtDNA "Common"-deletion subject 427.331