ProfileGDS1065 / 204112_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 58% 65% 60% 67% 58% 73% 64% 71% 59% 63% 57% 58% 60% 67% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16258
GSM24653Normal subject 28065
GSM24654Normal subject 383.860
GSM24655A3243G-MELAS subject 16167
GSM24656A3243G-MELAS subject 264.658
GSM24657A3243G-MELAS subject 3186.473
GSM24658A3243G-MELAS subject 472.864
GSM24659A3243G-PEO subject 182.971
GSM24660A3243G-PEO subject 259.459
GSM24661A3243G-PEO subject 353.863
GSM24662A3243G-PEO subject 45057
GSM24663mtDNA "Common"-deletion subject 16358
GSM24664mtDNA "Common"-deletion subject 212160
GSM24665mtDNA "Common"-deletion subject 3135.767
GSM24666mtDNA "Common"-deletion subject 4187.571