ProfileGDS1065 / 211628_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 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18887.299
GSM24653Normal subject 28116.499
GSM24654Normal subject 37808.199
GSM24655A3243G-MELAS subject 13162.499
GSM24656A3243G-MELAS subject 25186.299
GSM24657A3243G-MELAS subject 38843.599
GSM24658A3243G-MELAS subject 46564.299
GSM24659A3243G-PEO subject 16233.999
GSM24660A3243G-PEO subject 25412.999
GSM24661A3243G-PEO subject 36694.799
GSM24662A3243G-PEO subject 47914.199
GSM24663mtDNA "Common"-deletion subject 17818.699
GSM24664mtDNA "Common"-deletion subject 29440.799
GSM24665mtDNA "Common"-deletion subject 39985.599
GSM24666mtDNA "Common"-deletion subject 410546.399