ProfileGDS1065 / 218626_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 76% 80% 78% 80% 77% 84% 78% 76% 79% 82% 85% 80% 76% 79% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1146.476
GSM24653Normal subject 2165.580
GSM24654Normal subject 319778
GSM24655A3243G-MELAS subject 1114.880
GSM24656A3243G-MELAS subject 2147.177
GSM24657A3243G-MELAS subject 3381.284
GSM24658A3243G-MELAS subject 4154.278
GSM24659A3243G-PEO subject 1104.976
GSM24660A3243G-PEO subject 2150.579
GSM24661A3243G-PEO subject 3137.282
GSM24662A3243G-PEO subject 4213.585
GSM24663mtDNA "Common"-deletion subject 1186.380
GSM24664mtDNA "Common"-deletion subject 2258.876
GSM24665mtDNA "Common"-deletion subject 3254.979
GSM24666mtDNA "Common"-deletion subject 4371.182