ProfileGDS1065 / 213107_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 46% 49% 45% 41% 50% 43% 47% 54% 44% 51% 47% 55% 46% 52% 45% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13846
GSM24653Normal subject 241.249
GSM24654Normal subject 342.445
GSM24655A3243G-MELAS subject 122.541
GSM24656A3243G-MELAS subject 247.150
GSM24657A3243G-MELAS subject 346.543
GSM24658A3243G-MELAS subject 43547
GSM24659A3243G-PEO subject 142.954
GSM24660A3243G-PEO subject 232.744
GSM24661A3243G-PEO subject 332.351
GSM24662A3243G-PEO subject 433.847
GSM24663mtDNA "Common"-deletion subject 15555
GSM24664mtDNA "Common"-deletion subject 268.746
GSM24665mtDNA "Common"-deletion subject 370.552
GSM24666mtDNA "Common"-deletion subject 453.845