ProfileGDS1065 / 218470_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 55% 51% 57% 58% 48% 67% 53% 60% 55% 61% 59% 63% 55% 52% 61% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 154.755
GSM24653Normal subject 245.251
GSM24654Normal subject 371.157
GSM24655A3243G-MELAS subject 143.558
GSM24656A3243G-MELAS subject 243.648
GSM24657A3243G-MELAS subject 3140.767
GSM24658A3243G-MELAS subject 44553
GSM24659A3243G-PEO subject 154.460
GSM24660A3243G-PEO subject 250.455
GSM24661A3243G-PEO subject 349.861
GSM24662A3243G-PEO subject 452.959
GSM24663mtDNA "Common"-deletion subject 179.563
GSM24664mtDNA "Common"-deletion subject 294.155
GSM24665mtDNA "Common"-deletion subject 371.852
GSM24666mtDNA "Common"-deletion subject 4109.461