ProfileGDS1065 / 208649_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 92% 90% 94% 91% 93% 92% 94% 90% 91% 90% 92% 89% 91% 94% 92% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1590.292
GSM24653Normal subject 2405.190
GSM24654Normal subject 3899.594
GSM24655A3243G-MELAS subject 1281.391
GSM24656A3243G-MELAS subject 255993
GSM24657A3243G-MELAS subject 3843.992
GSM24658A3243G-MELAS subject 473794
GSM24659A3243G-PEO subject 1263.190
GSM24660A3243G-PEO subject 2419.491
GSM24661A3243G-PEO subject 326590
GSM24662A3243G-PEO subject 4398.892
GSM24663mtDNA "Common"-deletion subject 1377.289
GSM24664mtDNA "Common"-deletion subject 2758.791
GSM24665mtDNA "Common"-deletion subject 31127.594
GSM24666mtDNA "Common"-deletion subject 4921.292