ProfileGDS1065 / 212477_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 24% 26% 19% 27% 26% 14% 31% 29% 26% 9% 30% 21% 19% 23% 28% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112.124
GSM24653Normal subject 21326
GSM24654Normal subject 39.319
GSM24655A3243G-MELAS subject 111.127
GSM24656A3243G-MELAS subject 21526
GSM24657A3243G-MELAS subject 37.614
GSM24658A3243G-MELAS subject 415.831
GSM24659A3243G-PEO subject 114.929
GSM24660A3243G-PEO subject 21326
GSM24661A3243G-PEO subject 32.99
GSM24662A3243G-PEO subject 414.730
GSM24663mtDNA "Common"-deletion subject 19.721
GSM24664mtDNA "Common"-deletion subject 215.719
GSM24665mtDNA "Common"-deletion subject 316.123
GSM24666mtDNA "Common"-deletion subject 421.728