ProfileGDS1065 / 217438_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 19% 31% 6% 4% 24% 11% 22% 28% 7% 25% 10% 33% 9% 24% 23% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.519
GSM24653Normal subject 218.231
GSM24654Normal subject 336
GSM24655A3243G-MELAS subject 12.14
GSM24656A3243G-MELAS subject 213.724
GSM24657A3243G-MELAS subject 35.711
GSM24658A3243G-MELAS subject 48.722
GSM24659A3243G-PEO subject 113.828
GSM24660A3243G-PEO subject 23.27
GSM24661A3243G-PEO subject 38.525
GSM24662A3243G-PEO subject 43.610
GSM24663mtDNA "Common"-deletion subject 119.933
GSM24664mtDNA "Common"-deletion subject 26.69
GSM24665mtDNA "Common"-deletion subject 317.324
GSM24666mtDNA "Common"-deletion subject 415.623