ProfileGDS1065 / 217508_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 55% 55% 56% 52% 60% 51% 43% 54% 63% 52% 63% 68% 58% 55% 57% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 155.755
GSM24653Normal subject 252.555
GSM24654Normal subject 367.556
GSM24655A3243G-MELAS subject 134.552
GSM24656A3243G-MELAS subject 26960
GSM24657A3243G-MELAS subject 366.751
GSM24658A3243G-MELAS subject 429.643
GSM24659A3243G-PEO subject 142.754
GSM24660A3243G-PEO subject 26863
GSM24661A3243G-PEO subject 333.752
GSM24662A3243G-PEO subject 462.563
GSM24663mtDNA "Common"-deletion subject 198.368
GSM24664mtDNA "Common"-deletion subject 2110.158
GSM24665mtDNA "Common"-deletion subject 380.455
GSM24666mtDNA "Common"-deletion subject 490.757