ProfileGDS1065 / 219423_x_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 55% 42% 40% 11% 28% 33% 42% 15% 7% 29% 14% 44% 23% 18% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 154.355
GSM24653Normal subject 23042
GSM24654Normal subject 33340
GSM24655A3243G-MELAS subject 1411
GSM24656A3243G-MELAS subject 21728
GSM24657A3243G-MELAS subject 328.933
GSM24658A3243G-MELAS subject 427.642
GSM24659A3243G-PEO subject 16.215
GSM24660A3243G-PEO subject 23.37
GSM24661A3243G-PEO subject 311.429
GSM24662A3243G-PEO subject 44.814
GSM24663mtDNA "Common"-deletion subject 134.444
GSM24664mtDNA "Common"-deletion subject 220.423
GSM24665mtDNA "Common"-deletion subject 310.618
GSM24666mtDNA "Common"-deletion subject 430.633