ProfileGDS1065 / 216552_x_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 6% 12% 6% 15% 9% 7% 9% 11% 9% 14% 18% 13% 10% 18% 12% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 13.16
GSM24653Normal subject 2512
GSM24654Normal subject 33.36
GSM24655A3243G-MELAS subject 15.115
GSM24656A3243G-MELAS subject 24.59
GSM24657A3243G-MELAS subject 34.27
GSM24658A3243G-MELAS subject 43.19
GSM24659A3243G-PEO subject 14.711
GSM24660A3243G-PEO subject 249
GSM24661A3243G-PEO subject 34.414
GSM24662A3243G-PEO subject 46.818
GSM24663mtDNA "Common"-deletion subject 15.713
GSM24664mtDNA "Common"-deletion subject 27.510
GSM24665mtDNA "Common"-deletion subject 310.718
GSM24666mtDNA "Common"-deletion subject 46.612