ProfileGDS1065 / 201055_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 71% 54% 47% 78% 71% 66% 78% 77% 70% 72% 68% 59% 69% 60% 55% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1110.771
GSM24653Normal subject 250.154
GSM24654Normal subject 346.647
GSM24655A3243G-MELAS subject 199.178
GSM24656A3243G-MELAS subject 2111.571
GSM24657A3243G-MELAS subject 3132.166
GSM24658A3243G-MELAS subject 4152.278
GSM24659A3243G-PEO subject 1107.977
GSM24660A3243G-PEO subject 293.470
GSM24661A3243G-PEO subject 37872
GSM24662A3243G-PEO subject 478.368
GSM24663mtDNA "Common"-deletion subject 165.459
GSM24664mtDNA "Common"-deletion subject 2172.969
GSM24665mtDNA "Common"-deletion subject 39760
GSM24666mtDNA "Common"-deletion subject 480.555