ProfileGDS1065 / 202872_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 63% 65% 69% 62% 71% 72% 57% 57% 68% 70% 65% 59% 74% 74% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 176.763
GSM24653Normal subject 28065
GSM24654Normal subject 3126.769
GSM24655A3243G-MELAS subject 149.362
GSM24656A3243G-MELAS subject 2111.371
GSM24657A3243G-MELAS subject 3180.972
GSM24658A3243G-MELAS subject 453.557
GSM24659A3243G-PEO subject 14957
GSM24660A3243G-PEO subject 284.568
GSM24661A3243G-PEO subject 370.970
GSM24662A3243G-PEO subject 470.165
GSM24663mtDNA "Common"-deletion subject 167.359
GSM24664mtDNA "Common"-deletion subject 2232.774
GSM24665mtDNA "Common"-deletion subject 319074
GSM24666mtDNA "Common"-deletion subject 417971