ProfileGDS1065 / 202474_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 79% 66% 76% 81% 76% 70% 80% 84% 79% 78% 83% 80% 79% 71% 81% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1174.579
GSM24653Normal subject 283.666
GSM24654Normal subject 3175.776
GSM24655A3243G-MELAS subject 1122.481
GSM24656A3243G-MELAS subject 2143.476
GSM24657A3243G-MELAS subject 3161.670
GSM24658A3243G-MELAS subject 4174.480
GSM24659A3243G-PEO subject 1172.384
GSM24660A3243G-PEO subject 2151.379
GSM24661A3243G-PEO subject 3106.278
GSM24662A3243G-PEO subject 4179.483
GSM24663mtDNA "Common"-deletion subject 1184.280
GSM24664mtDNA "Common"-deletion subject 2298.979
GSM24665mtDNA "Common"-deletion subject 3168.471
GSM24666mtDNA "Common"-deletion subject 4330.981