ProfileGDS1065 / 218060_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 53% 67% 57% 26% 49% 70% 51% 59% 28% 62% 77% 70% 60% 33% 28% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 150.453
GSM24653Normal subject 286.367
GSM24654Normal subject 371.357
GSM24655A3243G-MELAS subject 110.926
GSM24656A3243G-MELAS subject 245.249
GSM24657A3243G-MELAS subject 3159.370
GSM24658A3243G-MELAS subject 441.151
GSM24659A3243G-PEO subject 152.959
GSM24660A3243G-PEO subject 214.828
GSM24661A3243G-PEO subject 351.562
GSM24662A3243G-PEO subject 4124.377
GSM24663mtDNA "Common"-deletion subject 1106.670
GSM24664mtDNA "Common"-deletion subject 2119.960
GSM24665mtDNA "Common"-deletion subject 329.533
GSM24666mtDNA "Common"-deletion subject 42328