ProfileGDS1065 / 204165_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 31% 37% 25% 34% 28% 30% 33% 19% 30% 33% 36% 33% 26% 27% 30% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 118.331
GSM24653Normal subject 22537
GSM24654Normal subject 313.925
GSM24655A3243G-MELAS subject 116.634
GSM24656A3243G-MELAS subject 216.728
GSM24657A3243G-MELAS subject 324.330
GSM24658A3243G-MELAS subject 417.933
GSM24659A3243G-PEO subject 18.419
GSM24660A3243G-PEO subject 216.330
GSM24661A3243G-PEO subject 313.933
GSM24662A3243G-PEO subject 421.236
GSM24663mtDNA "Common"-deletion subject 12033
GSM24664mtDNA "Common"-deletion subject 225.226
GSM24665mtDNA "Common"-deletion subject 321.327
GSM24666mtDNA "Common"-deletion subject 424.930