ProfileGDS1065 / 207177_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 9% 5% 4% 7% 1% 13% 1% 20% 4% 12% 13% 1% 2% 2% 12% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 149
GSM24653Normal subject 22.55
GSM24654Normal subject 32.34
GSM24655A3243G-MELAS subject 12.87
GSM24656A3243G-MELAS subject 21.51
GSM24657A3243G-MELAS subject 37.113
GSM24658A3243G-MELAS subject 40.91
GSM24659A3243G-PEO subject 18.520
GSM24660A3243G-PEO subject 22.44
GSM24661A3243G-PEO subject 33.712
GSM24662A3243G-PEO subject 44.513
GSM24663mtDNA "Common"-deletion subject 111
GSM24664mtDNA "Common"-deletion subject 232
GSM24665mtDNA "Common"-deletion subject 32.42
GSM24666mtDNA "Common"-deletion subject 46.612