ProfileGDS1065 / 207425_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 28% 30% 6% 48% 35% 29% 47% 29% 35% 22% 47% 6% 3% 8% 2% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 115.328
GSM24653Normal subject 216.730
GSM24654Normal subject 33.26
GSM24655A3243G-MELAS subject 129.948
GSM24656A3243G-MELAS subject 225.435
GSM24657A3243G-MELAS subject 322.629
GSM24658A3243G-MELAS subject 435.347
GSM24659A3243G-PEO subject 115.329
GSM24660A3243G-PEO subject 222.135
GSM24661A3243G-PEO subject 37.422
GSM24662A3243G-PEO subject 433.147
GSM24663mtDNA "Common"-deletion subject 13.16
GSM24664mtDNA "Common"-deletion subject 23.43
GSM24665mtDNA "Common"-deletion subject 358
GSM24666mtDNA "Common"-deletion subject 42.12