ProfileGDS1065 / 215062_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 52% 49% 52% 41% 42% 53% 50% 44% 52% 49% 55% 61% 52% 48% 47% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 148.652
GSM24653Normal subject 240.849
GSM24654Normal subject 358.452
GSM24655A3243G-MELAS subject 12341
GSM24656A3243G-MELAS subject 234.942
GSM24657A3243G-MELAS subject 371.853
GSM24658A3243G-MELAS subject 438.950
GSM24659A3243G-PEO subject 130.344
GSM24660A3243G-PEO subject 244.752
GSM24661A3243G-PEO subject 330.249
GSM24662A3243G-PEO subject 445.555
GSM24663mtDNA "Common"-deletion subject 171.561
GSM24664mtDNA "Common"-deletion subject 283.552
GSM24665mtDNA "Common"-deletion subject 360.548
GSM24666mtDNA "Common"-deletion subject 458.447