ProfileGDS1065 / 209426_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 72% 62% 61% 60% 50% 61% 50% 61% 62% 71% 64% 72% 53% 73% 56% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1116.372
GSM24653Normal subject 269.862
GSM24654Normal subject 384.561
GSM24655A3243G-MELAS subject 14660
GSM24656A3243G-MELAS subject 247.250
GSM24657A3243G-MELAS subject 3105.761
GSM24658A3243G-MELAS subject 439.150
GSM24659A3243G-PEO subject 156.561
GSM24660A3243G-PEO subject 265.962
GSM24661A3243G-PEO subject 374.571
GSM24662A3243G-PEO subject 467.264
GSM24663mtDNA "Common"-deletion subject 1117.872
GSM24664mtDNA "Common"-deletion subject 287.453
GSM24665mtDNA "Common"-deletion subject 3184.373
GSM24666mtDNA "Common"-deletion subject 486.656