ProfileGDS1065 / 206798_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 20% 33% 28% 25% 35% 22% 21% 30% 31% 24% 22% 54% 24% 32% 20% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.920
GSM24653Normal subject 220.233
GSM24654Normal subject 31728
GSM24655A3243G-MELAS subject 110.125
GSM24656A3243G-MELAS subject 224.935
GSM24657A3243G-MELAS subject 313.822
GSM24658A3243G-MELAS subject 47.921
GSM24659A3243G-PEO subject 115.830
GSM24660A3243G-PEO subject 217.431
GSM24661A3243G-PEO subject 38.424
GSM24662A3243G-PEO subject 48.922
GSM24663mtDNA "Common"-deletion subject 154.454
GSM24664mtDNA "Common"-deletion subject 221.424
GSM24665mtDNA "Common"-deletion subject 328.732
GSM24666mtDNA "Common"-deletion subject 412.920