ProfileGDS1065 / 206189_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 16% 7% 9% 33% 20% 11% 31% 35% 12% 28% 15% 15% 30% 31% 23% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.716
GSM24653Normal subject 23.27
GSM24654Normal subject 34.39
GSM24655A3243G-MELAS subject 115.633
GSM24656A3243G-MELAS subject 21020
GSM24657A3243G-MELAS subject 35.711
GSM24658A3243G-MELAS subject 415.731
GSM24659A3243G-PEO subject 12035
GSM24660A3243G-PEO subject 2512
GSM24661A3243G-PEO subject 310.428
GSM24662A3243G-PEO subject 45.515
GSM24663mtDNA "Common"-deletion subject 16.515
GSM24664mtDNA "Common"-deletion subject 231.830
GSM24665mtDNA "Common"-deletion subject 327.731
GSM24666mtDNA "Common"-deletion subject 415.223