ProfileGDS1065 / 221465_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 56% 62% 47% 66% 64% 50% 56% 53% 56% 60% 49% 43% 56% 45% 51% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 157.156
GSM24653Normal subject 267.462
GSM24654Normal subject 347.347
GSM24655A3243G-MELAS subject 158.766
GSM24656A3243G-MELAS subject 279.764
GSM24657A3243G-MELAS subject 363.350
GSM24658A3243G-MELAS subject 451.256
GSM24659A3243G-PEO subject 142.553
GSM24660A3243G-PEO subject 253.156
GSM24661A3243G-PEO subject 347.660
GSM24662A3243G-PEO subject 435.949
GSM24663mtDNA "Common"-deletion subject 134.143
GSM24664mtDNA "Common"-deletion subject 299.956
GSM24665mtDNA "Common"-deletion subject 35245
GSM24666mtDNA "Common"-deletion subject 47051