ProfileGDS1065 / 219421_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 73% 71% 80% 71% 80% 75% 71% 59% 67% 69% 63% 69% 75% 82% 79% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1121.673
GSM24653Normal subject 2102.971
GSM24654Normal subject 3225.680
GSM24655A3243G-MELAS subject 173.571
GSM24656A3243G-MELAS subject 2181.380
GSM24657A3243G-MELAS subject 3216.775
GSM24658A3243G-MELAS subject 4101.871
GSM24659A3243G-PEO subject 153.359
GSM24660A3243G-PEO subject 280.167
GSM24661A3243G-PEO subject 368.169
GSM24662A3243G-PEO subject 46363
GSM24663mtDNA "Common"-deletion subject 1103.669
GSM24664mtDNA "Common"-deletion subject 2245.475
GSM24665mtDNA "Common"-deletion subject 3321.982
GSM24666mtDNA "Common"-deletion subject 4296.979