ProfileGDS1065 / 211468_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% 2% 3% 8% 7% 1% 2% 1% 5% 4% 3% 5% 1% 13% 3% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.13
GSM24653Normal subject 21.62
GSM24654Normal subject 32.23
GSM24655A3243G-MELAS subject 138
GSM24656A3243G-MELAS subject 23.97
GSM24657A3243G-MELAS subject 31.51
GSM24658A3243G-MELAS subject 41.22
GSM24659A3243G-PEO subject 11.11
GSM24660A3243G-PEO subject 22.55
GSM24661A3243G-PEO subject 31.84
GSM24662A3243G-PEO subject 41.53
GSM24663mtDNA "Common"-deletion subject 12.75
GSM24664mtDNA "Common"-deletion subject 22.31
GSM24665mtDNA "Common"-deletion subject 37.713
GSM24666mtDNA "Common"-deletion subject 42.33