ProfileGDS1065 / 40189_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 93% 93% 93% 94% 94% 93% 93% 91% 94% 93% 91% 94% 94% 95% 94% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1642.993
GSM24653Normal subject 2601.693
GSM24654Normal subject 3785.393
GSM24655A3243G-MELAS subject 1446.894
GSM24656A3243G-MELAS subject 269994
GSM24657A3243G-MELAS subject 3992.593
GSM24658A3243G-MELAS subject 4586.793
GSM24659A3243G-PEO subject 1321.891
GSM24660A3243G-PEO subject 2581.494
GSM24661A3243G-PEO subject 3413.893
GSM24662A3243G-PEO subject 4348.891
GSM24663mtDNA "Common"-deletion subject 1829.994
GSM24664mtDNA "Common"-deletion subject 21247.794
GSM24665mtDNA "Common"-deletion subject 31378.495
GSM24666mtDNA "Common"-deletion subject 41268.694