ProfileGDS1065 / 201556_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 76% 62% 61% 71% 74% 74% 63% 70% 76% 74% 70% 63% 46% 69% 69% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1145.376
GSM24653Normal subject 267.562
GSM24654Normal subject 384.361
GSM24655A3243G-MELAS subject 17371
GSM24656A3243G-MELAS subject 2125.374
GSM24657A3243G-MELAS subject 3203.274
GSM24658A3243G-MELAS subject 46963
GSM24659A3243G-PEO subject 179.870
GSM24660A3243G-PEO subject 2125.476
GSM24661A3243G-PEO subject 386.974
GSM24662A3243G-PEO subject 48770
GSM24663mtDNA "Common"-deletion subject 178.163
GSM24664mtDNA "Common"-deletion subject 268.746
GSM24665mtDNA "Common"-deletion subject 315069
GSM24666mtDNA "Common"-deletion subject 4166.569