ProfileGDS1065 / 207492_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 26% 43% 44% 46% 46% 40% 42% 12% 40% 29% 41% 35% 36% 36% 39% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 113.226
GSM24653Normal subject 231.443
GSM24654Normal subject 341.344
GSM24655A3243G-MELAS subject 128.146
GSM24656A3243G-MELAS subject 240.646
GSM24657A3243G-MELAS subject 340.340
GSM24658A3243G-MELAS subject 428.442
GSM24659A3243G-PEO subject 14.912
GSM24660A3243G-PEO subject 227.840
GSM24661A3243G-PEO subject 31129
GSM24662A3243G-PEO subject 426.141
GSM24663mtDNA "Common"-deletion subject 122.335
GSM24664mtDNA "Common"-deletion subject 243.536
GSM24665mtDNA "Common"-deletion subject 335.536
GSM24666mtDNA "Common"-deletion subject 440.539