ProfileGDS1065 / 218908_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 71% 67% 62% 57% 61% 68% 66% 71% 67% 68% 69% 77% 63% 62% 71% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1111.471
GSM24653Normal subject 284.967
GSM24654Normal subject 389.862
GSM24655A3243G-MELAS subject 142.257
GSM24656A3243G-MELAS subject 27161
GSM24657A3243G-MELAS subject 3146.868
GSM24658A3243G-MELAS subject 48166
GSM24659A3243G-PEO subject 18571
GSM24660A3243G-PEO subject 282.667
GSM24661A3243G-PEO subject 365.868
GSM24662A3243G-PEO subject 481.469
GSM24663mtDNA "Common"-deletion subject 1157.577
GSM24664mtDNA "Common"-deletion subject 2134.163
GSM24665mtDNA "Common"-deletion subject 310762
GSM24666mtDNA "Common"-deletion subject 4182.871