ProfileGDS1065 / 211179_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 2% 1% 1% 3% 3% 1% 2% 16% 1% 4% 0% 1% 1% 2% 1% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.82
GSM24653Normal subject 21.21
GSM24654Normal subject 30.91
GSM24655A3243G-MELAS subject 11.63
GSM24656A3243G-MELAS subject 22.13
GSM24657A3243G-MELAS subject 31.11
GSM24658A3243G-MELAS subject 41.12
GSM24659A3243G-PEO subject 16.716
GSM24660A3243G-PEO subject 21.11
GSM24661A3243G-PEO subject 31.64
GSM24662A3243G-PEO subject 40.40
GSM24663mtDNA "Common"-deletion subject 11.21
GSM24664mtDNA "Common"-deletion subject 21.71
GSM24665mtDNA "Common"-deletion subject 32.12
GSM24666mtDNA "Common"-deletion subject 41.41