ProfileGDS1065 / 201288_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 83% 84% 82% 88% 82% 90% 88% 86% 81% 85% 84% 79% 85% 84% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1231.983
GSM24653Normal subject 2218.484
GSM24654Normal subject 325882
GSM24655A3243G-MELAS subject 1198.988
GSM24656A3243G-MELAS subject 2200.182
GSM24657A3243G-MELAS subject 369190
GSM24658A3243G-MELAS subject 4307.488
GSM24659A3243G-PEO subject 1195.786
GSM24660A3243G-PEO subject 2168.881
GSM24661A3243G-PEO subject 3172.785
GSM24662A3243G-PEO subject 4187.984
GSM24663mtDNA "Common"-deletion subject 1180.979
GSM24664mtDNA "Common"-deletion subject 2463.885
GSM24665mtDNA "Common"-deletion subject 3378.284
GSM24666mtDNA "Common"-deletion subject 4349.882