ProfileGDS1065 / 204552_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 17% 37% 52% 37% 49% 31% 35% 32% 39% 43% 19% 36% 49% 54% 34% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.517
GSM24653Normal subject 224.137
GSM24654Normal subject 357.752
GSM24655A3243G-MELAS subject 119.437
GSM24656A3243G-MELAS subject 245.349
GSM24657A3243G-MELAS subject 325.731
GSM24658A3243G-MELAS subject 42035
GSM24659A3243G-PEO subject 117.232
GSM24660A3243G-PEO subject 225.939
GSM24661A3243G-PEO subject 323.743
GSM24662A3243G-PEO subject 47.319
GSM24663mtDNA "Common"-deletion subject 124.236
GSM24664mtDNA "Common"-deletion subject 276.249
GSM24665mtDNA "Common"-deletion subject 376.654
GSM24666mtDNA "Common"-deletion subject 43234