ProfileGDS1065 / 207157_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 97% 98% 97% 98% 98% 97% 97% 97% 98% 97% 96% 98% 98% 98% 97% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11707.297
GSM24653Normal subject 22195.598
GSM24654Normal subject 32590.997
GSM24655A3243G-MELAS subject 11668.598
GSM24656A3243G-MELAS subject 22243.198
GSM24657A3243G-MELAS subject 32584.397
GSM24658A3243G-MELAS subject 41421.997
GSM24659A3243G-PEO subject 11065.497
GSM24660A3243G-PEO subject 21824.798
GSM24661A3243G-PEO subject 3119097
GSM24662A3243G-PEO subject 41058.996
GSM24663mtDNA "Common"-deletion subject 12222.498
GSM24664mtDNA "Common"-deletion subject 23403.198
GSM24665mtDNA "Common"-deletion subject 33403.298
GSM24666mtDNA "Common"-deletion subject 42710.897