ProfileGDS1065 / 216617_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 12% 5% 12% 4% 11% 42% 10% 12% 30% 24% 10% 11% 10% 11% 7% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1512
GSM24653Normal subject 22.75
GSM24654Normal subject 35.712
GSM24655A3243G-MELAS subject 11.94
GSM24656A3243G-MELAS subject 25.511
GSM24657A3243G-MELAS subject 344.642
GSM24658A3243G-MELAS subject 43.210
GSM24659A3243G-PEO subject 15.112
GSM24660A3243G-PEO subject 216.830
GSM24661A3243G-PEO subject 38.124
GSM24662A3243G-PEO subject 43.610
GSM24663mtDNA "Common"-deletion subject 14.611
GSM24664mtDNA "Common"-deletion subject 27.610
GSM24665mtDNA "Common"-deletion subject 36.311
GSM24666mtDNA "Common"-deletion subject 44.27