ProfileGDS1065 / 208304_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 11% 33% 36% 25% 30% 8% 37% 41% 34% 10% 40% 43% 35% 44% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.511
GSM24653Normal subject 220.533
GSM24654Normal subject 328.436
GSM24655A3243G-MELAS subject 19.825
GSM24656A3243G-MELAS subject 219.930
GSM24657A3243G-MELAS subject 34.78
GSM24658A3243G-MELAS subject 422.737
GSM24659A3243G-PEO subject 126.441
GSM24660A3243G-PEO subject 220.734
GSM24661A3243G-PEO subject 33.210
GSM24662A3243G-PEO subject 42540
GSM24663mtDNA "Common"-deletion subject 13343
GSM24664mtDNA "Common"-deletion subject 242.635
GSM24665mtDNA "Common"-deletion subject 350.644
GSM24666mtDNA "Common"-deletion subject 429.533