ProfileGDS1065 / 221559_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 69% 60% 73% 66% 64% 66% 71% 54% 63% 63% 57% 70% 69% 72% 85% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1100.569
GSM24653Normal subject 262.560
GSM24654Normal subject 3152.373
GSM24655A3243G-MELAS subject 157.966
GSM24656A3243G-MELAS subject 281.764
GSM24657A3243G-MELAS subject 3132.566
GSM24658A3243G-MELAS subject 4100.571
GSM24659A3243G-PEO subject 144.254
GSM24660A3243G-PEO subject 268.463
GSM24661A3243G-PEO subject 352.563
GSM24662A3243G-PEO subject 449.257
GSM24663mtDNA "Common"-deletion subject 1109.670
GSM24664mtDNA "Common"-deletion subject 2178.569
GSM24665mtDNA "Common"-deletion subject 3169.472
GSM24666mtDNA "Common"-deletion subject 4459.785