ProfileGDS1065 / 212264_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 80% 77% 79% 72% 77% 83% 79% 71% 78% 77% 77% 76% 80% 77% 81% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1184.580
GSM24653Normal subject 2144.877
GSM24654Normal subject 3218.379
GSM24655A3243G-MELAS subject 176.872
GSM24656A3243G-MELAS subject 2147.577
GSM24657A3243G-MELAS subject 3349.583
GSM24658A3243G-MELAS subject 4162.279
GSM24659A3243G-PEO subject 182.271
GSM24660A3243G-PEO subject 2134.678
GSM24661A3243G-PEO subject 3102.277
GSM24662A3243G-PEO subject 4124.477
GSM24663mtDNA "Common"-deletion subject 114876
GSM24664mtDNA "Common"-deletion subject 2327.880
GSM24665mtDNA "Common"-deletion subject 3227.877
GSM24666mtDNA "Common"-deletion subject 4337.381