ProfileGDS1065 / 209863_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 74% 72% 69% 68% 75% 68% 69% 72% 70% 72% 65% 66% 68% 67% 80% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1129.574
GSM24653Normal subject 2108.772
GSM24654Normal subject 3124.969
GSM24655A3243G-MELAS subject 164.868
GSM24656A3243G-MELAS subject 2133.775
GSM24657A3243G-MELAS subject 3149.468
GSM24658A3243G-MELAS subject 494.269
GSM24659A3243G-PEO subject 185.972
GSM24660A3243G-PEO subject 293.270
GSM24661A3243G-PEO subject 379.472
GSM24662A3243G-PEO subject 469.165
GSM24663mtDNA "Common"-deletion subject 188.766
GSM24664mtDNA "Common"-deletion subject 2168.368
GSM24665mtDNA "Common"-deletion subject 3132.767
GSM24666mtDNA "Common"-deletion subject 4323.980