ProfileGDS1065 / 211725_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 50% 52% 42% 62% 42% 63% 44% 61% 48% 50% 59% 57% 51% 50% 43% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 144.950
GSM24653Normal subject 245.752
GSM24654Normal subject 336.842
GSM24655A3243G-MELAS subject 149.662
GSM24656A3243G-MELAS subject 234.142
GSM24657A3243G-MELAS subject 3114.263
GSM24658A3243G-MELAS subject 430.344
GSM24659A3243G-PEO subject 156.161
GSM24660A3243G-PEO subject 238.548
GSM24661A3243G-PEO subject 33150
GSM24662A3243G-PEO subject 454.259
GSM24663mtDNA "Common"-deletion subject 160.757
GSM24664mtDNA "Common"-deletion subject 281.251
GSM24665mtDNA "Common"-deletion subject 364.850
GSM24666mtDNA "Common"-deletion subject 449.743