ProfileGDS1065 / 211896_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 92% 93% 96% 95% 92% 93% 95% 92% 92% 90% 89% 89% 92% 94% 93% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 156992
GSM24653Normal subject 2533.493
GSM24654Normal subject 31343.296
GSM24655A3243G-MELAS subject 1490.295
GSM24656A3243G-MELAS subject 248092
GSM24657A3243G-MELAS subject 3966.293
GSM24658A3243G-MELAS subject 4895.495
GSM24659A3243G-PEO subject 1367.192
GSM24660A3243G-PEO subject 2434.192
GSM24661A3243G-PEO subject 3274.590
GSM24662A3243G-PEO subject 4303.189
GSM24663mtDNA "Common"-deletion subject 1393.189
GSM24664mtDNA "Common"-deletion subject 2969.192
GSM24665mtDNA "Common"-deletion subject 31118.494
GSM24666mtDNA "Common"-deletion subject 41151.693