ProfileGDS1065 / 212519_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 93% 94% 93% 94% 94% 95% 95% 94% 93% 94% 92% 94% 94% 94% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1602.193
GSM24653Normal subject 2659.794
GSM24654Normal subject 3777.193
GSM24655A3243G-MELAS subject 1448.194
GSM24656A3243G-MELAS subject 2662.194
GSM24657A3243G-MELAS subject 31458.595
GSM24658A3243G-MELAS subject 4833.695
GSM24659A3243G-PEO subject 1481.794
GSM24660A3243G-PEO subject 2566.893
GSM24661A3243G-PEO subject 3499.994
GSM24662A3243G-PEO subject 4453.492
GSM24663mtDNA "Common"-deletion subject 1699.994
GSM24664mtDNA "Common"-deletion subject 21188.794
GSM24665mtDNA "Common"-deletion subject 31151.394
GSM24666mtDNA "Common"-deletion subject 41679.595