ProfileGDS1065 / 208927_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 80% 82% 84% 78% 87% 79% 82% 75% 86% 81% 85% 77% 83% 83% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1183.680
GSM24653Normal subject 2199.982
GSM24654Normal subject 3312.984
GSM24655A3243G-MELAS subject 1102.478
GSM24656A3243G-MELAS subject 2292.587
GSM24657A3243G-MELAS subject 3266.779
GSM24658A3243G-MELAS subject 4187.182
GSM24659A3243G-PEO subject 198.875
GSM24660A3243G-PEO subject 2239.986
GSM24661A3243G-PEO subject 3133.981
GSM24662A3243G-PEO subject 4215.385
GSM24663mtDNA "Common"-deletion subject 1152.677
GSM24664mtDNA "Common"-deletion subject 2380.583
GSM24665mtDNA "Common"-deletion subject 3344.983
GSM24666mtDNA "Common"-deletion subject 4502.486