ProfileGDS1065 / 215868_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 47% 36% 17% 23% 29% 36% 19% 29% 25% 36% 37% 11% 39% 36% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13947
GSM24653Normal subject 223.236
GSM24654Normal subject 38.217
GSM24655A3243G-MELAS subject 18.923
GSM24656A3243G-MELAS subject 218.929
GSM24657A3243G-MELAS subject 332.936
GSM24658A3243G-MELAS subject 46.919
GSM24659A3243G-PEO subject 114.729
GSM24660A3243G-PEO subject 21225
GSM24661A3243G-PEO subject 316.336
GSM24662A3243G-PEO subject 422.437
GSM24663mtDNA "Common"-deletion subject 14.611
GSM24664mtDNA "Common"-deletion subject 249.739
GSM24665mtDNA "Common"-deletion subject 335.236
GSM24666mtDNA "Common"-deletion subject 427.531