ProfileGDS1065 / 221407_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 68% 64% 62% 63% 77% 68% 61% 73% 72% 76% 53% 74% 64% 68% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 195.768
GSM24653Normal subject 275.964
GSM24654Normal subject 389.762
GSM24655A3243G-MELAS subject 151.263
GSM24656A3243G-MELAS subject 215077
GSM24657A3243G-MELAS subject 3143.368
GSM24658A3243G-MELAS subject 462.961
GSM24659A3243G-PEO subject 192.573
GSM24660A3243G-PEO subject 2103.472
GSM24661A3243G-PEO subject 397.676
GSM24662A3243G-PEO subject 441.853
GSM24663mtDNA "Common"-deletion subject 1130.874
GSM24664mtDNA "Common"-deletion subject 2143.864
GSM24665mtDNA "Common"-deletion subject 3142.968
GSM24666mtDNA "Common"-deletion subject 415868