ProfileGDS1065 / 201064_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% 97% 98% 98% 98% 97% 97% 97% 98% 97% 97% 97% 98% 98% 97% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12501.298
GSM24653Normal subject 21549.397
GSM24654Normal subject 33825.498
GSM24655A3243G-MELAS subject 11292.298
GSM24656A3243G-MELAS subject 22310.998
GSM24657A3243G-MELAS subject 33134.397
GSM24658A3243G-MELAS subject 41990.297
GSM24659A3243G-PEO subject 11318.597
GSM24660A3243G-PEO subject 22011.998
GSM24661A3243G-PEO subject 31350.697
GSM24662A3243G-PEO subject 41140.997
GSM24663mtDNA "Common"-deletion subject 11942.197
GSM24664mtDNA "Common"-deletion subject 23287.898
GSM24665mtDNA "Common"-deletion subject 34051.898
GSM24666mtDNA "Common"-deletion subject 43360.197