ProfileGDS1065 / 212021_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 59% 53% 58% 71% 70% 59% 63% 62% 71% 74% 53% 69% 61% 67% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 163.259
GSM24653Normal subject 24853
GSM24654Normal subject 373.858
GSM24655A3243G-MELAS subject 173.371
GSM24656A3243G-MELAS subject 2106.770
GSM24657A3243G-MELAS subject 396.759
GSM24658A3243G-MELAS subject 47063
GSM24659A3243G-PEO subject 15862
GSM24660A3243G-PEO subject 297.771
GSM24661A3243G-PEO subject 385.574
GSM24662A3243G-PEO subject 442.353
GSM24663mtDNA "Common"-deletion subject 1105.169
GSM24664mtDNA "Common"-deletion subject 2124.761
GSM24665mtDNA "Common"-deletion subject 3135.367
GSM24666mtDNA "Common"-deletion subject 473.452