ProfileGDS1065 / 34031_i_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 57% 43% 75% 32% 53% 57% 67% 39% 47% 38% 37% 47% 64% 68% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 158.957
GSM24653Normal subject 231.943
GSM24654Normal subject 3167.975
GSM24655A3243G-MELAS subject 115.432
GSM24656A3243G-MELAS subject 252.253
GSM24657A3243G-MELAS subject 387.357
GSM24658A3243G-MELAS subject 483.367
GSM24659A3243G-PEO subject 124.739
GSM24660A3243G-PEO subject 237.147
GSM24661A3243G-PEO subject 318.438
GSM24662A3243G-PEO subject 421.537
GSM24663mtDNA "Common"-deletion subject 14047
GSM24664mtDNA "Common"-deletion subject 2141.264
GSM24665mtDNA "Common"-deletion subject 3144.168
GSM24666mtDNA "Common"-deletion subject 4133.365