ProfileGDS1065 / 220158_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 58% 32% 59% 50% 42% 43% 41% 51% 57% 46% 49% 59% 53% 48% 42% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 161.658
GSM24653Normal subject 219.432
GSM24654Normal subject 379.459
GSM24655A3243G-MELAS subject 131.950
GSM24656A3243G-MELAS subject 233.842
GSM24657A3243G-MELAS subject 346.443
GSM24658A3243G-MELAS subject 426.641
GSM24659A3243G-PEO subject 138.351
GSM24660A3243G-PEO subject 255.357
GSM24661A3243G-PEO subject 326.646
GSM24662A3243G-PEO subject 435.349
GSM24663mtDNA "Common"-deletion subject 167.659
GSM24664mtDNA "Common"-deletion subject 290.153
GSM24665mtDNA "Common"-deletion subject 360.848
GSM24666mtDNA "Common"-deletion subject 44742