ProfileGDS1065 / 221467_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 48% 11% 31% 28% 45% 39% 25% 6% 40% 33% 39% 38% 31% 29% 35% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 140.748
GSM24653Normal subject 24.411
GSM24654Normal subject 320.631
GSM24655A3243G-MELAS subject 111.928
GSM24656A3243G-MELAS subject 239.245
GSM24657A3243G-MELAS subject 339.439
GSM24658A3243G-MELAS subject 410.825
GSM24659A3243G-PEO subject 13.26
GSM24660A3243G-PEO subject 227.540
GSM24661A3243G-PEO subject 314.333
GSM24662A3243G-PEO subject 423.739
GSM24663mtDNA "Common"-deletion subject 127.138
GSM24664mtDNA "Common"-deletion subject 232.731
GSM24665mtDNA "Common"-deletion subject 324.329
GSM24666mtDNA "Common"-deletion subject 433.735