ProfileGDS1065 / 222291_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 42% 52% 41% 33% 33% 48% 39% 56% 45% 56% 55% 48% 30% 39% 42% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13242
GSM24653Normal subject 245.352
GSM24654Normal subject 33641
GSM24655A3243G-MELAS subject 115.733
GSM24656A3243G-MELAS subject 222.233
GSM24657A3243G-MELAS subject 359.848
GSM24658A3243G-MELAS subject 42439
GSM24659A3243G-PEO subject 146.556
GSM24660A3243G-PEO subject 23445
GSM24661A3243G-PEO subject 34056
GSM24662A3243G-PEO subject 445.655
GSM24663mtDNA "Common"-deletion subject 141.548
GSM24664mtDNA "Common"-deletion subject 231.430
GSM24665mtDNA "Common"-deletion subject 34039
GSM24666mtDNA "Common"-deletion subject 446.942