ProfileGDS1065 / 218893_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 83% 86% 85% 91% 89% 92% 90% 93% 93% 93% 92% 90% 85% 85% 83% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1225.183
GSM24653Normal subject 2266.286
GSM24654Normal subject 3318.885
GSM24655A3243G-MELAS subject 126191
GSM24656A3243G-MELAS subject 2341.189
GSM24657A3243G-MELAS subject 3878.492
GSM24658A3243G-MELAS subject 4372.990
GSM24659A3243G-PEO subject 1397.193
GSM24660A3243G-PEO subject 2493.493
GSM24661A3243G-PEO subject 3428.293
GSM24662A3243G-PEO subject 4431.492
GSM24663mtDNA "Common"-deletion subject 141190
GSM24664mtDNA "Common"-deletion subject 2451.385
GSM24665mtDNA "Common"-deletion subject 3396.485
GSM24666mtDNA "Common"-deletion subject 4384.483