ProfileGDS1065 / 208049_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 11% 9% 36% 35% 24% 7% 24% 13% 13% 13% 9% 12% 24% 7% 36% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.411
GSM24653Normal subject 23.89
GSM24654Normal subject 327.836
GSM24655A3243G-MELAS subject 117.535
GSM24656A3243G-MELAS subject 213.124
GSM24657A3243G-MELAS subject 347
GSM24658A3243G-MELAS subject 49.924
GSM24659A3243G-PEO subject 15.713
GSM24660A3243G-PEO subject 25.413
GSM24661A3243G-PEO subject 34.113
GSM24662A3243G-PEO subject 43.49
GSM24663mtDNA "Common"-deletion subject 14.812
GSM24664mtDNA "Common"-deletion subject 221.324
GSM24665mtDNA "Common"-deletion subject 34.67
GSM24666mtDNA "Common"-deletion subject 435.836