ProfileGDS1065 / 202891_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 87% 84% 88% 90% 88% 86% 87% 90% 89% 89% 88% 84% 86% 84% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1309.487
GSM24653Normal subject 2224.284
GSM24654Normal subject 3414.988
GSM24655A3243G-MELAS subject 1253.290
GSM24656A3243G-MELAS subject 2307.488
GSM24657A3243G-MELAS subject 3464.986
GSM24658A3243G-MELAS subject 429787
GSM24659A3243G-PEO subject 1278.790
GSM24660A3243G-PEO subject 2325.789
GSM24661A3243G-PEO subject 3241.789
GSM24662A3243G-PEO subject 4273.988
GSM24663mtDNA "Common"-deletion subject 1254.984
GSM24664mtDNA "Common"-deletion subject 2478.886
GSM24665mtDNA "Common"-deletion subject 3376.284
GSM24666mtDNA "Common"-deletion subject 438183