ProfileGDS1065 / 206976_s_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% 90% 88% 91% 89% 86% 89% 86% 83% 86% 89% 89% 86% 88% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1329.887
GSM24653Normal subject 236590
GSM24654Normal subject 3445.288
GSM24655A3243G-MELAS subject 1274.391
GSM24656A3243G-MELAS subject 236289
GSM24657A3243G-MELAS subject 3461.286
GSM24658A3243G-MELAS subject 4330.289
GSM24659A3243G-PEO subject 1195.286
GSM24660A3243G-PEO subject 219683
GSM24661A3243G-PEO subject 3186.986
GSM24662A3243G-PEO subject 4284.489
GSM24663mtDNA "Common"-deletion subject 137989
GSM24664mtDNA "Common"-deletion subject 2486.186
GSM24665mtDNA "Common"-deletion subject 3521.988
GSM24666mtDNA "Common"-deletion subject 4605.288