ProfileGDS1065 / 210064_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 52% 57% 49% 63% 58% 50% 49% 51% 58% 57% 56% 60% 51% 57% 54% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14952
GSM24653Normal subject 256.457
GSM24654Normal subject 351.649
GSM24655A3243G-MELAS subject 151.363
GSM24656A3243G-MELAS subject 263.758
GSM24657A3243G-MELAS subject 363.350
GSM24658A3243G-MELAS subject 437.249
GSM24659A3243G-PEO subject 138.551
GSM24660A3243G-PEO subject 256.658
GSM24661A3243G-PEO subject 34257
GSM24662A3243G-PEO subject 447.556
GSM24663mtDNA "Common"-deletion subject 17060
GSM24664mtDNA "Common"-deletion subject 280.951
GSM24665mtDNA "Common"-deletion subject 386.957
GSM24666mtDNA "Common"-deletion subject 479.754