ProfileGDS1065 / 219569_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 64% 71% 63% 68% 67% 53% 60% 58% 55% 62% 58% 58% 69% 69% 62% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 180.864
GSM24653Normal subject 2103.671
GSM24654Normal subject 395.263
GSM24655A3243G-MELAS subject 164.768
GSM24656A3243G-MELAS subject 289.567
GSM24657A3243G-MELAS subject 374.453
GSM24658A3243G-MELAS subject 461.360
GSM24659A3243G-PEO subject 150.958
GSM24660A3243G-PEO subject 250.555
GSM24661A3243G-PEO subject 350.562
GSM24662A3243G-PEO subject 452.158
GSM24663mtDNA "Common"-deletion subject 162.458
GSM24664mtDNA "Common"-deletion subject 217369
GSM24665mtDNA "Common"-deletion subject 3146.569
GSM24666mtDNA "Common"-deletion subject 4116.662