ProfileGDS1065 / 201172_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 95% 96% 95% 96% 95% 95% 95% 95% 95% 95% 95% 96% 96% 96% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11030.695
GSM24653Normal subject 21249.996
GSM24654Normal subject 31294.695
GSM24655A3243G-MELAS subject 1730.696
GSM24656A3243G-MELAS subject 2905.795
GSM24657A3243G-MELAS subject 31615.895
GSM24658A3243G-MELAS subject 4824.295
GSM24659A3243G-PEO subject 1644.995
GSM24660A3243G-PEO subject 2714.895
GSM24661A3243G-PEO subject 3643.495
GSM24662A3243G-PEO subject 4825.595
GSM24663mtDNA "Common"-deletion subject 11124.796
GSM24664mtDNA "Common"-deletion subject 21935.196
GSM24665mtDNA "Common"-deletion subject 31818.196
GSM24666mtDNA "Common"-deletion subject 41661.895