ProfileGDS1065 / 202605_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 85% 85% 83% 88% 86% 86% 86% 91% 86% 86% 87% 88% 86% 81% 83% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1271.185
GSM24653Normal subject 2247.285
GSM24654Normal subject 3286.883
GSM24655A3243G-MELAS subject 1197.588
GSM24656A3243G-MELAS subject 227586
GSM24657A3243G-MELAS subject 3435.886
GSM24658A3243G-MELAS subject 4261.186
GSM24659A3243G-PEO subject 130391
GSM24660A3243G-PEO subject 2239.986
GSM24661A3243G-PEO subject 3191.786
GSM24662A3243G-PEO subject 4247.887
GSM24663mtDNA "Common"-deletion subject 1355.488
GSM24664mtDNA "Common"-deletion subject 2486.886
GSM24665mtDNA "Common"-deletion subject 3300.281
GSM24666mtDNA "Common"-deletion subject 438883