ProfileGDS1065 / 216902_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 2% 26% 26% 35% 13% 4% 31% 4% 9% 13% 5% 8% 21% 5% 26% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.42
GSM24653Normal subject 212.926
GSM24654Normal subject 31526
GSM24655A3243G-MELAS subject 117.935
GSM24656A3243G-MELAS subject 26.113
GSM24657A3243G-MELAS subject 32.74
GSM24658A3243G-MELAS subject 415.931
GSM24659A3243G-PEO subject 12.44
GSM24660A3243G-PEO subject 24.19
GSM24661A3243G-PEO subject 34.113
GSM24662A3243G-PEO subject 42.15
GSM24663mtDNA "Common"-deletion subject 13.58
GSM24664mtDNA "Common"-deletion subject 217.621
GSM24665mtDNA "Common"-deletion subject 33.65
GSM24666mtDNA "Common"-deletion subject 418.926