ProfileGDS1065 / 209747_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 69% 78% 77% 87% 74% 72% 70% 83% 75% 78% 77% 74% 73% 72% 62% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 198.369
GSM24653Normal subject 2152.878
GSM24654Normal subject 3192.177
GSM24655A3243G-MELAS subject 1180.987
GSM24656A3243G-MELAS subject 2125.374
GSM24657A3243G-MELAS subject 3177.672
GSM24658A3243G-MELAS subject 498.970
GSM24659A3243G-PEO subject 1157.183
GSM24660A3243G-PEO subject 2115.275
GSM24661A3243G-PEO subject 3108.978
GSM24662A3243G-PEO subject 4121.477
GSM24663mtDNA "Common"-deletion subject 113274
GSM24664mtDNA "Common"-deletion subject 2216.973
GSM24665mtDNA "Common"-deletion subject 3169.772
GSM24666mtDNA "Common"-deletion subject 4115.162