ProfileGDS1065 / 202381_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 72% 74% 73% 79% 81% 70% 75% 67% 66% 60% 62% 70% 79% 79% 76% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1118.972
GSM24653Normal subject 2119.774
GSM24654Normal subject 3149.873
GSM24655A3243G-MELAS subject 1108.379
GSM24656A3243G-MELAS subject 2184.981
GSM24657A3243G-MELAS subject 3164.670
GSM24658A3243G-MELAS subject 412375
GSM24659A3243G-PEO subject 170.567
GSM24660A3243G-PEO subject 278.966
GSM24661A3243G-PEO subject 347.460
GSM24662A3243G-PEO subject 46062
GSM24663mtDNA "Common"-deletion subject 1109.570
GSM24664mtDNA "Common"-deletion subject 2301.479
GSM24665mtDNA "Common"-deletion subject 3266.679
GSM24666mtDNA "Common"-deletion subject 4243.576