ProfileGDS1065 / 221544_s_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 25% 13% 27% 19% 33% 20% 13% 8% 21% 17% 9% 30% 27% 28% 12% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112.725
GSM24653Normal subject 25.213
GSM24654Normal subject 316.427
GSM24655A3243G-MELAS subject 16.919
GSM24656A3243G-MELAS subject 222.933
GSM24657A3243G-MELAS subject 311.920
GSM24658A3243G-MELAS subject 44.513
GSM24659A3243G-PEO subject 13.68
GSM24660A3243G-PEO subject 29.521
GSM24661A3243G-PEO subject 35.317
GSM24662A3243G-PEO subject 43.49
GSM24663mtDNA "Common"-deletion subject 11730
GSM24664mtDNA "Common"-deletion subject 22627
GSM24665mtDNA "Common"-deletion subject 321.928
GSM24666mtDNA "Common"-deletion subject 46.312