ProfileGDS1065 / 211052_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 78% 69% 47% 38% 63% 68% 76% 68% 55% 65% 72% 72% 65% 69% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1167.378
GSM24653Normal subject 295.769
GSM24654Normal subject 34647
GSM24655A3243G-MELAS subject 120.438
GSM24656A3243G-MELAS subject 279.263
GSM24657A3243G-MELAS subject 314768
GSM24658A3243G-MELAS subject 413476
GSM24659A3243G-PEO subject 172.768
GSM24660A3243G-PEO subject 251.255
GSM24661A3243G-PEO subject 358.465
GSM24662A3243G-PEO subject 49472
GSM24663mtDNA "Common"-deletion subject 1120.872
GSM24664mtDNA "Common"-deletion subject 2146.865
GSM24665mtDNA "Common"-deletion subject 3150.769
GSM24666mtDNA "Common"-deletion subject 4144.967