ProfileGDS1065 / 201345_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% 93% 93% 96% 92% 94% 92% 96% 95% 94% 94% 95% 94% 94% 93% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1805.694
GSM24653Normal subject 2608.893
GSM24654Normal subject 3795.793
GSM24655A3243G-MELAS subject 1624.196
GSM24656A3243G-MELAS subject 254592
GSM24657A3243G-MELAS subject 31168.794
GSM24658A3243G-MELAS subject 4484.192
GSM24659A3243G-PEO subject 1745.496
GSM24660A3243G-PEO subject 275895
GSM24661A3243G-PEO subject 3512.894
GSM24662A3243G-PEO subject 4579.694
GSM24663mtDNA "Common"-deletion subject 1104695
GSM24664mtDNA "Common"-deletion subject 21199.794
GSM24665mtDNA "Common"-deletion subject 31223.594
GSM24666mtDNA "Common"-deletion subject 4121693