ProfileGDS1065 / 210646_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 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% 100% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 116748.1100
GSM24653Normal subject 214101.4100
GSM24654Normal subject 315879.7100
GSM24655A3243G-MELAS subject 16370.9100
GSM24656A3243G-MELAS subject 29943.2100
GSM24657A3243G-MELAS subject 314654.7100
GSM24658A3243G-MELAS subject 413582.2100
GSM24659A3243G-PEO subject 110729.2100
GSM24660A3243G-PEO subject 211052.6100
GSM24661A3243G-PEO subject 311082.3100
GSM24662A3243G-PEO subject 412718.5100
GSM24663mtDNA "Common"-deletion subject 116331.2100
GSM24664mtDNA "Common"-deletion subject 217196.3100
GSM24665mtDNA "Common"-deletion subject 316835.5100
GSM24666mtDNA "Common"-deletion subject 417618.1100