ProfileGDS1065 / 209025_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% 62% 70% 74% 75% 69% 62% 51% 65% 63% 55% 63% 63% 68% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 154.655
GSM24653Normal subject 269.162
GSM24654Normal subject 3128.670
GSM24655A3243G-MELAS subject 181.674
GSM24656A3243G-MELAS subject 2131.375
GSM24657A3243G-MELAS subject 3151.969
GSM24658A3243G-MELAS subject 464.862
GSM24659A3243G-PEO subject 139.551
GSM24660A3243G-PEO subject 27365
GSM24661A3243G-PEO subject 351.963
GSM24662A3243G-PEO subject 445.155
GSM24663mtDNA "Common"-deletion subject 18063
GSM24664mtDNA "Common"-deletion subject 2133.563
GSM24665mtDNA "Common"-deletion subject 3143.368
GSM24666mtDNA "Common"-deletion subject 4157.668