ProfileGDS1065 / 208773_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 78% 80% 83% 78% 84% 76% 78% 74% 77% 75% 71% 78% 84% 83% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1164.778
GSM24653Normal subject 2168.680
GSM24654Normal subject 3273.983
GSM24655A3243G-MELAS subject 199.778
GSM24656A3243G-MELAS subject 2226.184
GSM24657A3243G-MELAS subject 323076
GSM24658A3243G-MELAS subject 415078
GSM24659A3243G-PEO subject 196.374
GSM24660A3243G-PEO subject 2132.177
GSM24661A3243G-PEO subject 390.875
GSM24662A3243G-PEO subject 489.571
GSM24663mtDNA "Common"-deletion subject 1167.178
GSM24664mtDNA "Common"-deletion subject 2432.684
GSM24665mtDNA "Common"-deletion subject 3340.783
GSM24666mtDNA "Common"-deletion subject 4365.482