ProfileGDS1065 / 203374_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 59% 71% 83% 79% 73% 70% 72% 72% 69% 71% 65% 73% 78% 73% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 164.259
GSM24653Normal subject 2105.871
GSM24654Normal subject 3285.283
GSM24655A3243G-MELAS subject 1106.679
GSM24656A3243G-MELAS subject 211973
GSM24657A3243G-MELAS subject 3166.370
GSM24658A3243G-MELAS subject 4107.772
GSM24659A3243G-PEO subject 187.472
GSM24660A3243G-PEO subject 288.569
GSM24661A3243G-PEO subject 375.771
GSM24662A3243G-PEO subject 468.665
GSM24663mtDNA "Common"-deletion subject 1127.473
GSM24664mtDNA "Common"-deletion subject 2284.478
GSM24665mtDNA "Common"-deletion subject 3186.573
GSM24666mtDNA "Common"-deletion subject 4157.268