ProfileGDS1065 / 214342_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 23% 11% 24% 13% 11% 14% 17% 15% 21% 7% 16% 24% 16% 25% 11% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 111.423
GSM24653Normal subject 24.711
GSM24654Normal subject 312.824
GSM24655A3243G-MELAS subject 14.713
GSM24656A3243G-MELAS subject 25.411
GSM24657A3243G-MELAS subject 37.514
GSM24658A3243G-MELAS subject 46.217
GSM24659A3243G-PEO subject 16.515
GSM24660A3243G-PEO subject 29.421
GSM24661A3243G-PEO subject 32.37
GSM24662A3243G-PEO subject 45.816
GSM24663mtDNA "Common"-deletion subject 111.224
GSM24664mtDNA "Common"-deletion subject 212.216
GSM24665mtDNA "Common"-deletion subject 317.725
GSM24666mtDNA "Common"-deletion subject 45.811