ProfileGDS1065 / 217863_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% 59% 66% 55% 73% 77% 68% 57% 63% 65% 76% 67% 74% 71% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 188.866
GSM24653Normal subject 260.559
GSM24654Normal subject 3105.266
GSM24655A3243G-MELAS subject 138.655
GSM24656A3243G-MELAS subject 2120.773
GSM24657A3243G-MELAS subject 3238.877
GSM24658A3243G-MELAS subject 486.168
GSM24659A3243G-PEO subject 147.857
GSM24660A3243G-PEO subject 268.563
GSM24661A3243G-PEO subject 357.265
GSM24662A3243G-PEO subject 4120.776
GSM24663mtDNA "Common"-deletion subject 194.967
GSM24664mtDNA "Common"-deletion subject 2230.774
GSM24665mtDNA "Common"-deletion subject 3166.571
GSM24666mtDNA "Common"-deletion subject 4376.683