ProfileGDS1065 / 220708_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 62% 57% 53% 55% 55% 51% 56% 60% 53% 60% 51% 59% 55% 56% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 172.162
GSM24653Normal subject 256.257
GSM24654Normal subject 360.453
GSM24655A3243G-MELAS subject 13955
GSM24656A3243G-MELAS subject 256.955
GSM24657A3243G-MELAS subject 366.951
GSM24658A3243G-MELAS subject 450.156
GSM24659A3243G-PEO subject 154.460
GSM24660A3243G-PEO subject 245.753
GSM24661A3243G-PEO subject 346.260
GSM24662A3243G-PEO subject 43951
GSM24663mtDNA "Common"-deletion subject 165.159
GSM24664mtDNA "Common"-deletion subject 29655
GSM24665mtDNA "Common"-deletion subject 38556
GSM24666mtDNA "Common"-deletion subject 472.152