ProfileGDS1065 / 217594_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 7% 10% 24% 16% 15% 1% 1% 9% 1% 1% 18% 2% 4% 20% 24% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.37
GSM24653Normal subject 24.210
GSM24654Normal subject 31324
GSM24655A3243G-MELAS subject 15.416
GSM24656A3243G-MELAS subject 2715
GSM24657A3243G-MELAS subject 311
GSM24658A3243G-MELAS subject 40.81
GSM24659A3243G-PEO subject 14.29
GSM24660A3243G-PEO subject 21.21
GSM24661A3243G-PEO subject 30.71
GSM24662A3243G-PEO subject 46.818
GSM24663mtDNA "Common"-deletion subject 11.42
GSM24664mtDNA "Common"-deletion subject 244
GSM24665mtDNA "Common"-deletion subject 312.320
GSM24666mtDNA "Common"-deletion subject 417.324