ProfileGDS1065 / 210797_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 67% 68% 50% 63% 67% 57% 66% 77% 67% 69% 66% 68% 68% 61% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 189.267
GSM24653Normal subject 29168
GSM24654Normal subject 35250
GSM24655A3243G-MELAS subject 152.263
GSM24656A3243G-MELAS subject 291.467
GSM24657A3243G-MELAS subject 385.857
GSM24658A3243G-MELAS subject 47866
GSM24659A3243G-PEO subject 1111.677
GSM24660A3243G-PEO subject 280.967
GSM24661A3243G-PEO subject 370.169
GSM24662A3243G-PEO subject 470.766
GSM24663mtDNA "Common"-deletion subject 196.568
GSM24664mtDNA "Common"-deletion subject 2165.368
GSM24665mtDNA "Common"-deletion subject 3102.761
GSM24666mtDNA "Common"-deletion subject 496.959