ProfileGDS1065 / 202930_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 93% 93% 95% 93% 95% 94% 93% 91% 93% 93% 88% 93% 94% 95% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1699.593
GSM24653Normal subject 2555.593
GSM24654Normal subject 31236.995
GSM24655A3243G-MELAS subject 135493
GSM24656A3243G-MELAS subject 2767.695
GSM24657A3243G-MELAS subject 31169.794
GSM24658A3243G-MELAS subject 4624.693
GSM24659A3243G-PEO subject 1302.791
GSM24660A3243G-PEO subject 2557.893
GSM24661A3243G-PEO subject 3413.793
GSM24662A3243G-PEO subject 4258.588
GSM24663mtDNA "Common"-deletion subject 1626.493
GSM24664mtDNA "Common"-deletion subject 21228.694
GSM24665mtDNA "Common"-deletion subject 31465.595
GSM24666mtDNA "Common"-deletion subject 41627.395