ProfileGDS1065 / 218420_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 57% 62% 57% 62% 59% 61% 62% 56% 58% 53% 68% 58% 56% 60% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 158.857
GSM24653Normal subject 268.262
GSM24654Normal subject 371.457
GSM24655A3243G-MELAS subject 149.562
GSM24656A3243G-MELAS subject 266.559
GSM24657A3243G-MELAS subject 3104.161
GSM24658A3243G-MELAS subject 467.162
GSM24659A3243G-PEO subject 147.556
GSM24660A3243G-PEO subject 257.358
GSM24661A3243G-PEO subject 335.953
GSM24662A3243G-PEO subject 476.768
GSM24663mtDNA "Common"-deletion subject 163.358
GSM24664mtDNA "Common"-deletion subject 298.156
GSM24665mtDNA "Common"-deletion subject 399.560
GSM24666mtDNA "Common"-deletion subject 494.258