ProfileGDS1065 / 211473_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 17% 11% 28% 16% 24% 24% 18% 23% 15% 11% 19% 16% 16% 16% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.517
GSM24653Normal subject 24.511
GSM24654Normal subject 317.528
GSM24655A3243G-MELAS subject 15.616
GSM24656A3243G-MELAS subject 213.324
GSM24657A3243G-MELAS subject 315.824
GSM24658A3243G-MELAS subject 46.418
GSM24659A3243G-PEO subject 110.823
GSM24660A3243G-PEO subject 26.515
GSM24661A3243G-PEO subject 33.511
GSM24662A3243G-PEO subject 46.919
GSM24663mtDNA "Common"-deletion subject 16.916
GSM24664mtDNA "Common"-deletion subject 211.816
GSM24665mtDNA "Common"-deletion subject 39.516
GSM24666mtDNA "Common"-deletion subject 4814