ProfileGDS1065 / 213369_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 19% 18% 7% 5% 11% 18% 14% 10% 5% 6% 3% 7% 3% 4% 4% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.519
GSM24653Normal subject 27.318
GSM24654Normal subject 33.67
GSM24655A3243G-MELAS subject 12.25
GSM24656A3243G-MELAS subject 25.211
GSM24657A3243G-MELAS subject 31018
GSM24658A3243G-MELAS subject 44.714
GSM24659A3243G-PEO subject 14.510
GSM24660A3243G-PEO subject 22.75
GSM24661A3243G-PEO subject 326
GSM24662A3243G-PEO subject 41.73
GSM24663mtDNA "Common"-deletion subject 13.37
GSM24664mtDNA "Common"-deletion subject 23.63
GSM24665mtDNA "Common"-deletion subject 33.14
GSM24666mtDNA "Common"-deletion subject 42.94