ProfileGDS1065 / 213438_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% 62% 43% 43% 48% 60% 52% 38% 40% 39% 41% 57% 52% 46% 48% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 167.560
GSM24653Normal subject 269.862
GSM24654Normal subject 338.243
GSM24655A3243G-MELAS subject 124.843
GSM24656A3243G-MELAS subject 24348
GSM24657A3243G-MELAS subject 399.160
GSM24658A3243G-MELAS subject 442.252
GSM24659A3243G-PEO subject 123.438
GSM24660A3243G-PEO subject 226.940
GSM24661A3243G-PEO subject 319.539
GSM24662A3243G-PEO subject 425.941
GSM24663mtDNA "Common"-deletion subject 159.957
GSM24664mtDNA "Common"-deletion subject 284.852
GSM24665mtDNA "Common"-deletion subject 354.746
GSM24666mtDNA "Common"-deletion subject 461.748