ProfileGDS1065 / 219596_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 57% 57% 60% 65% 55% 54% 53% 60% 56% 48% 55% 68% 71% 62% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 159.757
GSM24653Normal subject 256.857
GSM24654Normal subject 380.660
GSM24655A3243G-MELAS subject 156.265
GSM24656A3243G-MELAS subject 256.955
GSM24657A3243G-MELAS subject 37754
GSM24658A3243G-MELAS subject 445.353
GSM24659A3243G-PEO subject 153.560
GSM24660A3243G-PEO subject 251.956
GSM24661A3243G-PEO subject 329.248
GSM24662A3243G-PEO subject 44655
GSM24663mtDNA "Common"-deletion subject 196.468
GSM24664mtDNA "Common"-deletion subject 219071
GSM24665mtDNA "Common"-deletion subject 3109.762
GSM24666mtDNA "Common"-deletion subject 4187.171