ProfileGDS1065 / 209850_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 68% 61% 47% 47% 34% 69% 71% 65% 61% 68% 72% 39% 36% 51% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 196.468
GSM24653Normal subject 266.661
GSM24654Normal subject 346.247
GSM24655A3243G-MELAS subject 129.347
GSM24656A3243G-MELAS subject 223.634
GSM24657A3243G-MELAS subject 3155.869
GSM24658A3243G-MELAS subject 4102.671
GSM24659A3243G-PEO subject 165.665
GSM24660A3243G-PEO subject 26261
GSM24661A3243G-PEO subject 366.568
GSM24662A3243G-PEO subject 494.972
GSM24663mtDNA "Common"-deletion subject 12839
GSM24664mtDNA "Common"-deletion subject 244.736
GSM24665mtDNA "Common"-deletion subject 369.451
GSM24666mtDNA "Common"-deletion subject 496.759