ProfileGDS1065 / 218472_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 82% 78% 84% 84% 80% 81% 83% 77% 83% 85% 80% 81% 80% 84% 85% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 120682
GSM24653Normal subject 2151.578
GSM24654Normal subject 3295.684
GSM24655A3243G-MELAS subject 1142.284
GSM24656A3243G-MELAS subject 2183.380
GSM24657A3243G-MELAS subject 3318.581
GSM24658A3243G-MELAS subject 421183
GSM24659A3243G-PEO subject 1107.377
GSM24660A3243G-PEO subject 2197.183
GSM24661A3243G-PEO subject 3171.385
GSM24662A3243G-PEO subject 4146.280
GSM24663mtDNA "Common"-deletion subject 1201.581
GSM24664mtDNA "Common"-deletion subject 2323.980
GSM24665mtDNA "Common"-deletion subject 3378.184
GSM24666mtDNA "Common"-deletion subject 4442.285