ProfileGDS1065 / 213806_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 16% 13% 12% 16% 14% 14% 12% 15% 15% 17% 16% 17% 12% 15% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.816
GSM24653Normal subject 25.313
GSM24654Normal subject 35.512
GSM24655A3243G-MELAS subject 15.616
GSM24656A3243G-MELAS subject 26.914
GSM24657A3243G-MELAS subject 37.414
GSM24658A3243G-MELAS subject 4412
GSM24659A3243G-PEO subject 16.415
GSM24660A3243G-PEO subject 26.415
GSM24661A3243G-PEO subject 35.417
GSM24662A3243G-PEO subject 4616
GSM24663mtDNA "Common"-deletion subject 17.317
GSM24664mtDNA "Common"-deletion subject 28.912
GSM24665mtDNA "Common"-deletion subject 38.815
GSM24666mtDNA "Common"-deletion subject 47.514