ProfileGDS1065 / 204324_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 33% 15% 35% 7% 34% 34% 38% 26% 20% 32% 38% 31% 28% 30% 30% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 120.433
GSM24653Normal subject 26.215
GSM24654Normal subject 326.935
GSM24655A3243G-MELAS subject 12.87
GSM24656A3243G-MELAS subject 224.434
GSM24657A3243G-MELAS subject 33034
GSM24658A3243G-MELAS subject 422.838
GSM24659A3243G-PEO subject 112.526
GSM24660A3243G-PEO subject 28.720
GSM24661A3243G-PEO subject 313.332
GSM24662A3243G-PEO subject 42338
GSM24663mtDNA "Common"-deletion subject 118.131
GSM24664mtDNA "Common"-deletion subject 228.528
GSM24665mtDNA "Common"-deletion subject 325.930
GSM24666mtDNA "Common"-deletion subject 424.930