ProfileGDS1065 / 205683_x_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 60% 65% 60% 67% 65% 75% 78% 80% 69% 67% 69% 71% 61% 55% 63% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 166.560
GSM24653Normal subject 279.765
GSM24654Normal subject 383.560
GSM24655A3243G-MELAS subject 160.467
GSM24656A3243G-MELAS subject 28465
GSM24657A3243G-MELAS subject 3211.875
GSM24658A3243G-MELAS subject 4150.978
GSM24659A3243G-PEO subject 1129.880
GSM24660A3243G-PEO subject 288.969
GSM24661A3243G-PEO subject 363.267
GSM24662A3243G-PEO subject 480.569
GSM24663mtDNA "Common"-deletion subject 1114.271
GSM24664mtDNA "Common"-deletion subject 2123.961
GSM24665mtDNA "Common"-deletion subject 381.855
GSM24666mtDNA "Common"-deletion subject 4121.863