ProfileGDS1065 / 206412_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% 31% 8% 21% 11% 42% 22% 6% 26% 24% 19% 19% 37% 14% 23% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 123
GSM24653Normal subject 218.531
GSM24654Normal subject 33.98
GSM24655A3243G-MELAS subject 17.821
GSM24656A3243G-MELAS subject 25.411
GSM24657A3243G-MELAS subject 34642
GSM24658A3243G-MELAS subject 48.622
GSM24659A3243G-PEO subject 13.16
GSM24660A3243G-PEO subject 213.126
GSM24661A3243G-PEO subject 38.424
GSM24662A3243G-PEO subject 47.119
GSM24663mtDNA "Common"-deletion subject 18.219
GSM24664mtDNA "Common"-deletion subject 246.337
GSM24665mtDNA "Common"-deletion subject 37.914
GSM24666mtDNA "Common"-deletion subject 416.123