ProfileGDS1065 / 203968_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 20% 27% 39% 37% 29% 27% 25% 21% 26% 23% 11% 36% 20% 33% 27% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 18.820
GSM24653Normal subject 213.927
GSM24654Normal subject 331.939
GSM24655A3243G-MELAS subject 118.937
GSM24656A3243G-MELAS subject 218.829
GSM24657A3243G-MELAS subject 32027
GSM24658A3243G-MELAS subject 41125
GSM24659A3243G-PEO subject 19.521
GSM24660A3243G-PEO subject 213.426
GSM24661A3243G-PEO subject 37.523
GSM24662A3243G-PEO subject 43.811
GSM24663mtDNA "Common"-deletion subject 123.536
GSM24664mtDNA "Common"-deletion subject 216.320
GSM24665mtDNA "Common"-deletion subject 330.533
GSM24666mtDNA "Common"-deletion subject 421.227