ProfileGDS1065 / 201479_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 87% 88% 88% 89% 88% 89% 88% 88% 88% 89% 89% 90% 88% 88% 90% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 131587
GSM24653Normal subject 231788
GSM24654Normal subject 3435.888
GSM24655A3243G-MELAS subject 1208.389
GSM24656A3243G-MELAS subject 2322.188
GSM24657A3243G-MELAS subject 3570.589
GSM24658A3243G-MELAS subject 4326.188
GSM24659A3243G-PEO subject 1234.188
GSM24660A3243G-PEO subject 2288.688
GSM24661A3243G-PEO subject 3250.189
GSM24662A3243G-PEO subject 4292.289
GSM24663mtDNA "Common"-deletion subject 1439.190
GSM24664mtDNA "Common"-deletion subject 2564.788
GSM24665mtDNA "Common"-deletion subject 3562.488
GSM24666mtDNA "Common"-deletion subject 4765.890