ProfileGDS1065 / 205807_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 76% 69% 62% 76% 74% 70% 64% 75% 77% 76% 75% 59% 70% 67% 76% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1149.376
GSM24653Normal subject 295.969
GSM24654Normal subject 389.162
GSM24655A3243G-MELAS subject 191.176
GSM24656A3243G-MELAS subject 2126.274
GSM24657A3243G-MELAS subject 316170
GSM24658A3243G-MELAS subject 47364
GSM24659A3243G-PEO subject 198.675
GSM24660A3243G-PEO subject 213177
GSM24661A3243G-PEO subject 399.176
GSM24662A3243G-PEO subject 4110.375
GSM24663mtDNA "Common"-deletion subject 166.159
GSM24664mtDNA "Common"-deletion subject 2187.770
GSM24665mtDNA "Common"-deletion subject 3137.767
GSM24666mtDNA "Common"-deletion subject 4241.676