ProfileGDS1065 / 218752_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 38% 38% 41% 26% 33% 55% 57% 43% 34% 38% 33% 35% 31% 38% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 126.538
GSM24653Normal subject 225.138
GSM24654Normal subject 335.241
GSM24655A3243G-MELAS subject 110.726
GSM24656A3243G-MELAS subject 223.133
GSM24657A3243G-MELAS subject 380.555
GSM24658A3243G-MELAS subject 452.957
GSM24659A3243G-PEO subject 128.843
GSM24660A3243G-PEO subject 220.934
GSM24661A3243G-PEO subject 318.238
GSM24662A3243G-PEO subject 418.133
GSM24663mtDNA "Common"-deletion subject 122.335
GSM24664mtDNA "Common"-deletion subject 23331
GSM24665mtDNA "Common"-deletion subject 337.938
GSM24666mtDNA "Common"-deletion subject 484.456