ProfileGDS1065 / 209016_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 3% 8% 13% 26% 24% 3% 17% 6% 8% 9% 2% 11% 2% 10% 7% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 123
GSM24653Normal subject 23.58
GSM24654Normal subject 3613
GSM24655A3243G-MELAS subject 110.926
GSM24656A3243G-MELAS subject 213.524
GSM24657A3243G-MELAS subject 32.23
GSM24658A3243G-MELAS subject 45.917
GSM24659A3243G-PEO subject 13.26
GSM24660A3243G-PEO subject 23.48
GSM24661A3243G-PEO subject 32.89
GSM24662A3243G-PEO subject 41.42
GSM24663mtDNA "Common"-deletion subject 14.711
GSM24664mtDNA "Common"-deletion subject 22.82
GSM24665mtDNA "Common"-deletion subject 3610
GSM24666mtDNA "Common"-deletion subject 447