ProfileGDS1065 / 202171_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 77% 72% 87% 64% 83% 71% 77% 70% 79% 72% 65% 71% 81% 82% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1158.577
GSM24653Normal subject 2108.972
GSM24654Normal subject 3384.287
GSM24655A3243G-MELAS subject 154.964
GSM24656A3243G-MELAS subject 2212.983
GSM24657A3243G-MELAS subject 3169.771
GSM24658A3243G-MELAS subject 4144.677
GSM24659A3243G-PEO subject 181.270
GSM24660A3243G-PEO subject 2149.779
GSM24661A3243G-PEO subject 377.572
GSM24662A3243G-PEO subject 468.165
GSM24663mtDNA "Common"-deletion subject 1111.671
GSM24664mtDNA "Common"-deletion subject 2345.481
GSM24665mtDNA "Common"-deletion subject 3323.182
GSM24666mtDNA "Common"-deletion subject 4373.182