ProfileGDS1065 / 206617_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 7% 11% 17% 12% 16% 12% 10% 26% 13% 6% 10% 13% 9% 21% 10% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 13.27
GSM24653Normal subject 24.711
GSM24654Normal subject 38.117
GSM24655A3243G-MELAS subject 14.112
GSM24656A3243G-MELAS subject 27.516
GSM24657A3243G-MELAS subject 36.412
GSM24658A3243G-MELAS subject 43.410
GSM24659A3243G-PEO subject 112.126
GSM24660A3243G-PEO subject 25.313
GSM24661A3243G-PEO subject 32.26
GSM24662A3243G-PEO subject 43.610
GSM24663mtDNA "Common"-deletion subject 15.513
GSM24664mtDNA "Common"-deletion subject 26.99
GSM24665mtDNA "Common"-deletion subject 313.421
GSM24666mtDNA "Common"-deletion subject 45.310