ProfileGDS1065 / 201701_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 66% 72% 63% 68% 72% 83% 63% 72% 67% 85% 79% 71% 63% 61% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 188.666
GSM24653Normal subject 2108.672
GSM24654Normal subject 393.563
GSM24655A3243G-MELAS subject 163.468
GSM24656A3243G-MELAS subject 2117.672
GSM24657A3243G-MELAS subject 3358.283
GSM24658A3243G-MELAS subject 470.563
GSM24659A3243G-PEO subject 186.972
GSM24660A3243G-PEO subject 280.867
GSM24661A3243G-PEO subject 3174.385
GSM24662A3243G-PEO subject 4141.579
GSM24663mtDNA "Common"-deletion subject 1114.671
GSM24664mtDNA "Common"-deletion subject 2133.463
GSM24665mtDNA "Common"-deletion subject 3103.561
GSM24666mtDNA "Common"-deletion subject 418671