ProfileGDS1065 / 201308_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 8% 9% 1% 27% 5% 13% 26% 23% 17% 7% 2% 2% 23% 15% 18% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 13.68
GSM24653Normal subject 23.99
GSM24654Normal subject 31.31
GSM24655A3243G-MELAS subject 111.127
GSM24656A3243G-MELAS subject 235
GSM24657A3243G-MELAS subject 37.113
GSM24658A3243G-MELAS subject 411.626
GSM24659A3243G-PEO subject 110.423
GSM24660A3243G-PEO subject 27.317
GSM24661A3243G-PEO subject 32.57
GSM24662A3243G-PEO subject 41.12
GSM24663mtDNA "Common"-deletion subject 11.62
GSM24664mtDNA "Common"-deletion subject 22023
GSM24665mtDNA "Common"-deletion subject 39.115
GSM24666mtDNA "Common"-deletion subject 410.518