ProfileGDS1065 / 203381_s_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 49% 53% 64% 57% 47% 57% 61% 62% 45% 46% 43% 42% 39% 54% 50% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 14349
GSM24653Normal subject 247.553
GSM24654Normal subject 396.964
GSM24655A3243G-MELAS subject 141.457
GSM24656A3243G-MELAS subject 241.847
GSM24657A3243G-MELAS subject 386.157
GSM24658A3243G-MELAS subject 462.861
GSM24659A3243G-PEO subject 158.562
GSM24660A3243G-PEO subject 234.545
GSM24661A3243G-PEO subject 326.246
GSM24662A3243G-PEO subject 427.743
GSM24663mtDNA "Common"-deletion subject 132.442
GSM24664mtDNA "Common"-deletion subject 250.139
GSM24665mtDNA "Common"-deletion subject 378.554
GSM24666mtDNA "Common"-deletion subject 466.450