ProfileGDS1065 / 219700_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 74% 57% 62% 58% 51% 68% 51% 63% 58% 70% 63% 69% 25% 71% 51% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1127.874
GSM24653Normal subject 25657
GSM24654Normal subject 388.462
GSM24655A3243G-MELAS subject 143.858
GSM24656A3243G-MELAS subject 248.451
GSM24657A3243G-MELAS subject 314468
GSM24658A3243G-MELAS subject 441.851
GSM24659A3243G-PEO subject 159.863
GSM24660A3243G-PEO subject 257.658
GSM24661A3243G-PEO subject 371.670
GSM24662A3243G-PEO subject 463.663
GSM24663mtDNA "Common"-deletion subject 1103.869
GSM24664mtDNA "Common"-deletion subject 223.225
GSM24665mtDNA "Common"-deletion subject 316771
GSM24666mtDNA "Common"-deletion subject 469.551