ProfileGDS1065 / 205278_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 6% 20% 4% 14% 24% 6% 9% 3% 17% 3% 4% 26% 5% 22% 6% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.96
GSM24653Normal subject 28.720
GSM24654Normal subject 32.64
GSM24655A3243G-MELAS subject 1514
GSM24656A3243G-MELAS subject 213.524
GSM24657A3243G-MELAS subject 33.76
GSM24658A3243G-MELAS subject 43.19
GSM24659A3243G-PEO subject 11.93
GSM24660A3243G-PEO subject 27.217
GSM24661A3243G-PEO subject 31.43
GSM24662A3243G-PEO subject 41.84
GSM24663mtDNA "Common"-deletion subject 113.526
GSM24664mtDNA "Common"-deletion subject 24.45
GSM24665mtDNA "Common"-deletion subject 315.122
GSM24666mtDNA "Common"-deletion subject 43.86