ProfileGDS1065 / 205003_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 70% 71% 70% 64% 77% 70% 77% 65% 64% 74% 69% 74% 75% 81% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1106.470
GSM24653Normal subject 2101.171
GSM24654Normal subject 3129.370
GSM24655A3243G-MELAS subject 15564
GSM24656A3243G-MELAS subject 2153.677
GSM24657A3243G-MELAS subject 3160.670
GSM24658A3243G-MELAS subject 4138.677
GSM24659A3243G-PEO subject 165.265
GSM24660A3243G-PEO subject 270.864
GSM24661A3243G-PEO subject 389.374
GSM24662A3243G-PEO subject 482.969
GSM24663mtDNA "Common"-deletion subject 1131.474
GSM24664mtDNA "Common"-deletion subject 2246.175
GSM24665mtDNA "Common"-deletion subject 3306.381
GSM24666mtDNA "Common"-deletion subject 4389.783