ProfileGDS1065 / 218395_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 74% 77% 76% 73% 77% 77% 72% 58% 77% 68% 72% 71% 82% 80% 81% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112974
GSM24653Normal subject 2143.377
GSM24654Normal subject 3181.376
GSM24655A3243G-MELAS subject 177.873
GSM24656A3243G-MELAS subject 2151.277
GSM24657A3243G-MELAS subject 3239.777
GSM24658A3243G-MELAS subject 4109.772
GSM24659A3243G-PEO subject 150.258
GSM24660A3243G-PEO subject 213277
GSM24661A3243G-PEO subject 365.568
GSM24662A3243G-PEO subject 492.472
GSM24663mtDNA "Common"-deletion subject 1112.971
GSM24664mtDNA "Common"-deletion subject 2365.182
GSM24665mtDNA "Common"-deletion subject 3283.580
GSM24666mtDNA "Common"-deletion subject 4344.881