ProfileGDS1065 / 212057_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% 57% 75% 65% 70% 68% 69% 70% 69% 56% 57% 58% 67% 69% 63% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 186.266
GSM24653Normal subject 255.857
GSM24654Normal subject 3172.475
GSM24655A3243G-MELAS subject 155.865
GSM24656A3243G-MELAS subject 2104.270
GSM24657A3243G-MELAS subject 3146.268
GSM24658A3243G-MELAS subject 494.969
GSM24659A3243G-PEO subject 18070
GSM24660A3243G-PEO subject 288.669
GSM24661A3243G-PEO subject 340.156
GSM24662A3243G-PEO subject 449.957
GSM24663mtDNA "Common"-deletion subject 163.258
GSM24664mtDNA "Common"-deletion subject 2158.667
GSM24665mtDNA "Common"-deletion subject 3150.269
GSM24666mtDNA "Common"-deletion subject 4122.763