ProfileGDS1065 / 217207_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 63% 77% 66% 73% 80% 56% 68% 77% 69% 71% 59% 65% 70% 72% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 176.363
GSM24653Normal subject 2138.377
GSM24654Normal subject 310966
GSM24655A3243G-MELAS subject 177.773
GSM24656A3243G-MELAS subject 2172.880
GSM24657A3243G-MELAS subject 383.656
GSM24658A3243G-MELAS subject 489.368
GSM24659A3243G-PEO subject 111377
GSM24660A3243G-PEO subject 289.869
GSM24661A3243G-PEO subject 374.171
GSM24662A3243G-PEO subject 454.359
GSM24663mtDNA "Common"-deletion subject 185.465
GSM24664mtDNA "Common"-deletion subject 218870
GSM24665mtDNA "Common"-deletion subject 3172.672
GSM24666mtDNA "Common"-deletion subject 487.756