ProfileGDS1065 / 217377_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 69% 70% 61% 70% 65% 57% 51% 74% 54% 59% 66% 61% 69% 58% 51% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 199.769
GSM24653Normal subject 297.270
GSM24654Normal subject 386.861
GSM24655A3243G-MELAS subject 168.770
GSM24656A3243G-MELAS subject 283.965
GSM24657A3243G-MELAS subject 388.957
GSM24658A3243G-MELAS subject 441.651
GSM24659A3243G-PEO subject 196.274
GSM24660A3243G-PEO subject 248.954
GSM24661A3243G-PEO subject 346.159
GSM24662A3243G-PEO subject 472.166
GSM24663mtDNA "Common"-deletion subject 173.661
GSM24664mtDNA "Common"-deletion subject 2180.669
GSM24665mtDNA "Common"-deletion subject 390.458
GSM24666mtDNA "Common"-deletion subject 470.551