ProfileGDS1065 / 209724_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 52% 48% 62% 42% 41% 56% 56% 46% 53% 54% 61% 47% 46% 50% 63% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 147.252
GSM24653Normal subject 239.148
GSM24654Normal subject 39062
GSM24655A3243G-MELAS subject 123.642
GSM24656A3243G-MELAS subject 233.141
GSM24657A3243G-MELAS subject 384.956
GSM24658A3243G-MELAS subject 450.256
GSM24659A3243G-PEO subject 13346
GSM24660A3243G-PEO subject 246.653
GSM24661A3243G-PEO subject 33754
GSM24662A3243G-PEO subject 45961
GSM24663mtDNA "Common"-deletion subject 140.847
GSM24664mtDNA "Common"-deletion subject 266.446
GSM24665mtDNA "Common"-deletion subject 364.150
GSM24666mtDNA "Common"-deletion subject 4120.263