ProfileGDS1065 / 202984_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 3% 32% 38% 26% 29% 34% 31% 21% 23% 19% 24% 2% 16% 1% 24% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.13
GSM24653Normal subject 218.932
GSM24654Normal subject 331.338
GSM24655A3243G-MELAS subject 110.726
GSM24656A3243G-MELAS subject 218.529
GSM24657A3243G-MELAS subject 329.734
GSM24658A3243G-MELAS subject 415.931
GSM24659A3243G-PEO subject 1921
GSM24660A3243G-PEO subject 21123
GSM24661A3243G-PEO subject 3619
GSM24662A3243G-PEO subject 410.124
GSM24663mtDNA "Common"-deletion subject 11.42
GSM24664mtDNA "Common"-deletion subject 212.316
GSM24665mtDNA "Common"-deletion subject 31.71
GSM24666mtDNA "Common"-deletion subject 416.724