ProfileGDS1065 / 204807_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 54% 38% 63% 52% 61% 46% 52% 45% 55% 47% 42% 53% 64% 50% 55% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 152.154
GSM24653Normal subject 225.138
GSM24654Normal subject 393.363
GSM24655A3243G-MELAS subject 135.152
GSM24656A3243G-MELAS subject 271.461
GSM24657A3243G-MELAS subject 353.446
GSM24658A3243G-MELAS subject 443.252
GSM24659A3243G-PEO subject 131.845
GSM24660A3243G-PEO subject 250.455
GSM24661A3243G-PEO subject 328.447
GSM24662A3243G-PEO subject 426.942
GSM24663mtDNA "Common"-deletion subject 152.153
GSM24664mtDNA "Common"-deletion subject 2137.964
GSM24665mtDNA "Common"-deletion subject 366.150
GSM24666mtDNA "Common"-deletion subject 482.855