ProfileGDS1065 / 205083_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 60% 49% 65% 55% 48% 47% 61% 62% 51% 63% 51% 57% 51% 53% 56% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 166.760
GSM24653Normal subject 240.749
GSM24654Normal subject 3102.865
GSM24655A3243G-MELAS subject 138.255
GSM24656A3243G-MELAS subject 24448
GSM24657A3243G-MELAS subject 356.647
GSM24658A3243G-MELAS subject 462.261
GSM24659A3243G-PEO subject 159.262
GSM24660A3243G-PEO subject 243.551
GSM24661A3243G-PEO subject 353.963
GSM24662A3243G-PEO subject 438.751
GSM24663mtDNA "Common"-deletion subject 161.357
GSM24664mtDNA "Common"-deletion subject 280.551
GSM24665mtDNA "Common"-deletion subject 374.153
GSM24666mtDNA "Common"-deletion subject 486.456