ProfileGDS1065 / 210084_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 28% 21% 41% 17% 40% 68% 65% 65% 47% 50% 42% 14% 14% 17% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11528
GSM24653Normal subject 29.221
GSM24654Normal subject 334.941
GSM24655A3243G-MELAS subject 16.117
GSM24656A3243G-MELAS subject 23240
GSM24657A3243G-MELAS subject 3148.868
GSM24658A3243G-MELAS subject 477.765
GSM24659A3243G-PEO subject 16665
GSM24660A3243G-PEO subject 236.647
GSM24661A3243G-PEO subject 331.650
GSM24662A3243G-PEO subject 427.242
GSM24663mtDNA "Common"-deletion subject 16.114
GSM24664mtDNA "Common"-deletion subject 210.714
GSM24665mtDNA "Common"-deletion subject 310.317
GSM24666mtDNA "Common"-deletion subject 449.443