ProfileGDS1065 / 202756_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 91% 89% 87% 91% 91% 89% 91% 93% 92% 94% 94% 92% 89% 87% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1499.291
GSM24653Normal subject 2333.889
GSM24654Normal subject 3384.587
GSM24655A3243G-MELAS subject 127291
GSM24656A3243G-MELAS subject 2448.191
GSM24657A3243G-MELAS subject 3571.589
GSM24658A3243G-MELAS subject 4414.391
GSM24659A3243G-PEO subject 143793
GSM24660A3243G-PEO subject 2467.792
GSM24661A3243G-PEO subject 3475.894
GSM24662A3243G-PEO subject 4560.394
GSM24663mtDNA "Common"-deletion subject 1550.692
GSM24664mtDNA "Common"-deletion subject 2637.189
GSM24665mtDNA "Common"-deletion subject 3513.687
GSM24666mtDNA "Common"-deletion subject 4602.488