ProfileGDS1065 / 204052_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 44% 73% 69% 54% 47% 60% 66% 67% 44% 80% 74% 53% 34% 54% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 135.344
GSM24653Normal subject 2114.873
GSM24654Normal subject 3123.169
GSM24655A3243G-MELAS subject 137.454
GSM24656A3243G-MELAS subject 242.347
GSM24657A3243G-MELAS subject 397.760
GSM24658A3243G-MELAS subject 481.366
GSM24659A3243G-PEO subject 171.767
GSM24660A3243G-PEO subject 232.644
GSM24661A3243G-PEO subject 3123.480
GSM24662A3243G-PEO subject 4104.174
GSM24663mtDNA "Common"-deletion subject 150.853
GSM24664mtDNA "Common"-deletion subject 23934
GSM24665mtDNA "Common"-deletion subject 378.354
GSM24666mtDNA "Common"-deletion subject 486.156