ProfileGDS1065 / 213868_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 12% 11% 14% 15% 17% 20% 11% 8% 2% 18% 11% 19% 9% 23% 15% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15.212
GSM24653Normal subject 24.511
GSM24654Normal subject 36.414
GSM24655A3243G-MELAS subject 15.115
GSM24656A3243G-MELAS subject 2817
GSM24657A3243G-MELAS subject 312.120
GSM24658A3243G-MELAS subject 43.811
GSM24659A3243G-PEO subject 13.68
GSM24660A3243G-PEO subject 21.42
GSM24661A3243G-PEO subject 35.518
GSM24662A3243G-PEO subject 4411
GSM24663mtDNA "Common"-deletion subject 18.219
GSM24664mtDNA "Common"-deletion subject 279
GSM24665mtDNA "Common"-deletion subject 315.923
GSM24666mtDNA "Common"-deletion subject 48.215