ProfileGDS1065 / 216344_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 60% 43% 35% 24% 30% 42% 33% 33% 40% 45% 43% 42% 44% 26% 38% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 165.960
GSM24653Normal subject 232.443
GSM24654Normal subject 326.135
GSM24655A3243G-MELAS subject 19.424
GSM24656A3243G-MELAS subject 219.930
GSM24657A3243G-MELAS subject 345.942
GSM24658A3243G-MELAS subject 417.733
GSM24659A3243G-PEO subject 118.233
GSM24660A3243G-PEO subject 227.340
GSM24661A3243G-PEO subject 325.945
GSM24662A3243G-PEO subject 428.943
GSM24663mtDNA "Common"-deletion subject 131.742
GSM24664mtDNA "Common"-deletion subject 260.644
GSM24665mtDNA "Common"-deletion subject 319.126
GSM24666mtDNA "Common"-deletion subject 438.738