ProfileGDS1065 / 215100_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% 64% 61% 69% 69% 55% 63% 77% 72% 67% 68% 58% 65% 61% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18966
GSM24653Normal subject 273.664
GSM24654Normal subject 385.761
GSM24655A3243G-MELAS subject 167.569
GSM24656A3243G-MELAS subject 2100.969
GSM24657A3243G-MELAS subject 380.155
GSM24658A3243G-MELAS subject 470.663
GSM24659A3243G-PEO subject 1112.877
GSM24660A3243G-PEO subject 2102.572
GSM24661A3243G-PEO subject 362.167
GSM24662A3243G-PEO subject 478.768
GSM24663mtDNA "Common"-deletion subject 164.858
GSM24664mtDNA "Common"-deletion subject 2144.365
GSM24665mtDNA "Common"-deletion subject 3104.161
GSM24666mtDNA "Common"-deletion subject 485.256