ProfileGDS1065 / 217852_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 94% 94% 93% 94% 95% 94% 93% 94% 93% 92% 93% 94% 95% 94% 94% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1702.294
GSM24653Normal subject 2655.894
GSM24654Normal subject 3853.293
GSM24655A3243G-MELAS subject 1452.494
GSM24656A3243G-MELAS subject 2786.495
GSM24657A3243G-MELAS subject 31106.594
GSM24658A3243G-MELAS subject 4564.593
GSM24659A3243G-PEO subject 1510.994
GSM24660A3243G-PEO subject 2547.793
GSM24661A3243G-PEO subject 336192
GSM24662A3243G-PEO subject 4539.793
GSM24663mtDNA "Common"-deletion subject 1733.594
GSM24664mtDNA "Common"-deletion subject 2149695
GSM24665mtDNA "Common"-deletion subject 31135.794
GSM24666mtDNA "Common"-deletion subject 41434.294