ProfileGDS1065 / 203296_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 98% 98% 98% 98% 99% 98% 98% 98% 98% 98% 98% 98% 99% 98% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1370898
GSM24653Normal subject 23540.198
GSM24654Normal subject 33809.798
GSM24655A3243G-MELAS subject 11842.698
GSM24656A3243G-MELAS subject 23775.999
GSM24657A3243G-MELAS subject 34846.198
GSM24658A3243G-MELAS subject 43580.498
GSM24659A3243G-PEO subject 11984.698
GSM24660A3243G-PEO subject 22645.598
GSM24661A3243G-PEO subject 32235.198
GSM24662A3243G-PEO subject 42242.498
GSM24663mtDNA "Common"-deletion subject 13815.998
GSM24664mtDNA "Common"-deletion subject 26820.499
GSM24665mtDNA "Common"-deletion subject 35195.498
GSM24666mtDNA "Common"-deletion subject 46590.799