ProfileGDS1065 / 220079_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 85% 88% 84% 88% 88% 90% 87% 90% 88% 87% 90% 91% 90% 80% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1271.985
GSM24653Normal subject 2305.188
GSM24654Normal subject 3295.984
GSM24655A3243G-MELAS subject 1204.888
GSM24656A3243G-MELAS subject 2328.888
GSM24657A3243G-MELAS subject 3700.990
GSM24658A3243G-MELAS subject 4295.587
GSM24659A3243G-PEO subject 1274.390
GSM24660A3243G-PEO subject 2277.488
GSM24661A3243G-PEO subject 3202.987
GSM24662A3243G-PEO subject 4312.590
GSM24663mtDNA "Common"-deletion subject 1495.391
GSM24664mtDNA "Common"-deletion subject 2728.790
GSM24665mtDNA "Common"-deletion subject 3286.380
GSM24666mtDNA "Common"-deletion subject 4602.688