ProfileGDS1065 / 40829_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% 92% 91% 94% 94% 93% 91% 96% 95% 95% 95% 93% 90% 90% 91% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 167893
GSM24653Normal subject 2464.592
GSM24654Normal subject 3634.691
GSM24655A3243G-MELAS subject 1421.294
GSM24656A3243G-MELAS subject 2653.794
GSM24657A3243G-MELAS subject 31005.493
GSM24658A3243G-MELAS subject 4430.491
GSM24659A3243G-PEO subject 1700.196
GSM24660A3243G-PEO subject 272395
GSM24661A3243G-PEO subject 3551.195
GSM24662A3243G-PEO subject 4689.595
GSM24663mtDNA "Common"-deletion subject 1656.993
GSM24664mtDNA "Common"-deletion subject 2739.290
GSM24665mtDNA "Common"-deletion subject 3653.890
GSM24666mtDNA "Common"-deletion subject 4813.191