ProfileGDS1065 / 217165_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 90% 91% 94% 89% 92% 93% 89% 88% 92% 90% 90% 90% 94% 89% 93% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1441.990
GSM24653Normal subject 2440.891
GSM24654Normal subject 31022.694
GSM24655A3243G-MELAS subject 1216.689
GSM24656A3243G-MELAS subject 2477.592
GSM24657A3243G-MELAS subject 3928.393
GSM24658A3243G-MELAS subject 4336.389
GSM24659A3243G-PEO subject 123288
GSM24660A3243G-PEO subject 2433.792
GSM24661A3243G-PEO subject 3286.990
GSM24662A3243G-PEO subject 4324.790
GSM24663mtDNA "Common"-deletion subject 1420.690
GSM24664mtDNA "Common"-deletion subject 21172.994
GSM24665mtDNA "Common"-deletion subject 3581.189
GSM24666mtDNA "Common"-deletion subject 41183.393