ProfileGDS1065 / 219167_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 84% 79% 79% 79% 77% 80% 73% 83% 79% 82% 75% 84% 77% 77% 80% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 125084
GSM24653Normal subject 2161.579
GSM24654Normal subject 3215.479
GSM24655A3243G-MELAS subject 1107.179
GSM24656A3243G-MELAS subject 2153.777
GSM24657A3243G-MELAS subject 3284.880
GSM24658A3243G-MELAS subject 4115.673
GSM24659A3243G-PEO subject 115483
GSM24660A3243G-PEO subject 2151.379
GSM24661A3243G-PEO subject 3139.382
GSM24662A3243G-PEO subject 4112.375
GSM24663mtDNA "Common"-deletion subject 125284
GSM24664mtDNA "Common"-deletion subject 2260.377
GSM24665mtDNA "Common"-deletion subject 3231.577
GSM24666mtDNA "Common"-deletion subject 4308.780