ProfileGDS1065 / 212324_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 46% 58% 64% 56% 66% 53% 64% 44% 49% 48% 55% 54% 58% 57% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 137.646
GSM24653Normal subject 258.158
GSM24654Normal subject 397.764
GSM24655A3243G-MELAS subject 140.156
GSM24656A3243G-MELAS subject 288.766
GSM24657A3243G-MELAS subject 372.553
GSM24658A3243G-MELAS subject 472.664
GSM24659A3243G-PEO subject 130.544
GSM24660A3243G-PEO subject 239.749
GSM24661A3243G-PEO subject 329.648
GSM24662A3243G-PEO subject 446.355
GSM24663mtDNA "Common"-deletion subject 154.354
GSM24664mtDNA "Common"-deletion subject 2107.458
GSM24665mtDNA "Common"-deletion subject 387.757
GSM24666mtDNA "Common"-deletion subject 492.858