ProfileGDS1065 / 206158_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 98% 98% 99% 98% 98% 98% 98% 97% 98% 97% 98% 97% 98% 98% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12537.798
GSM24653Normal subject 22560.798
GSM24654Normal subject 35092.199
GSM24655A3243G-MELAS subject 11880.598
GSM24656A3243G-MELAS subject 22954.498
GSM24657A3243G-MELAS subject 34727.498
GSM24658A3243G-MELAS subject 43031.498
GSM24659A3243G-PEO subject 11450.797
GSM24660A3243G-PEO subject 22503.498
GSM24661A3243G-PEO subject 31423.897
GSM24662A3243G-PEO subject 42224.698
GSM24663mtDNA "Common"-deletion subject 12060.897
GSM24664mtDNA "Common"-deletion subject 2458098
GSM24665mtDNA "Common"-deletion subject 35296.398
GSM24666mtDNA "Common"-deletion subject 45189.998