ProfileGDS1065 / 204155_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 62% 59% 74% 62% 63% 51% 67% 53% 72% 55% 56% 60% 69% 69% 64% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 171.962
GSM24653Normal subject 260.159
GSM24654Normal subject 3160.774
GSM24655A3243G-MELAS subject 149.362
GSM24656A3243G-MELAS subject 277.663
GSM24657A3243G-MELAS subject 366.351
GSM24658A3243G-MELAS subject 485.867
GSM24659A3243G-PEO subject 142.153
GSM24660A3243G-PEO subject 2100.672
GSM24661A3243G-PEO subject 338.855
GSM24662A3243G-PEO subject 447.556
GSM24663mtDNA "Common"-deletion subject 168.960
GSM24664mtDNA "Common"-deletion subject 2176.169
GSM24665mtDNA "Common"-deletion subject 3152.769
GSM24666mtDNA "Common"-deletion subject 4127.664