ProfileGDS1065 / 221312_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 14% 12% 11% 7% 6% 8% 12% 9% 38% 30% 9% 10% 11% 22% 10% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 15.814
GSM24653Normal subject 24.912
GSM24654Normal subject 35.111
GSM24655A3243G-MELAS subject 12.77
GSM24656A3243G-MELAS subject 23.56
GSM24657A3243G-MELAS subject 34.78
GSM24658A3243G-MELAS subject 44.212
GSM24659A3243G-PEO subject 149
GSM24660A3243G-PEO subject 225.438
GSM24661A3243G-PEO subject 311.830
GSM24662A3243G-PEO subject 43.29
GSM24663mtDNA "Common"-deletion subject 14.410
GSM24664mtDNA "Common"-deletion subject 28.111
GSM24665mtDNA "Common"-deletion subject 314.822
GSM24666mtDNA "Common"-deletion subject 45.510