ProfileGDS1065 / 207577_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 39% 32% 39% 40% 43% 34% 28% 54% 43% 44% 42% 42% 40% 39% 34% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 127.839
GSM24653Normal subject 219.332
GSM24654Normal subject 331.839
GSM24655A3243G-MELAS subject 122.140
GSM24656A3243G-MELAS subject 236.143
GSM24657A3243G-MELAS subject 330.734
GSM24658A3243G-MELAS subject 412.828
GSM24659A3243G-PEO subject 14454
GSM24660A3243G-PEO subject 231.443
GSM24661A3243G-PEO subject 324.744
GSM24662A3243G-PEO subject 427.242
GSM24663mtDNA "Common"-deletion subject 131.742
GSM24664mtDNA "Common"-deletion subject 252.440
GSM24665mtDNA "Common"-deletion subject 340.139
GSM24666mtDNA "Common"-deletion subject 430.834