ProfileGDS1065 / 37004_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 46% 38% 39% 50% 35% 35% 39% 42% 45% 37% 37% 53% 31% 35% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 137.646
GSM24653Normal subject 226.138
GSM24654Normal subject 332.439
GSM24655A3243G-MELAS subject 132.950
GSM24656A3243G-MELAS subject 225.535
GSM24657A3243G-MELAS subject 332.435
GSM24658A3243G-MELAS subject 424.839
GSM24659A3243G-PEO subject 12842
GSM24660A3243G-PEO subject 233.845
GSM24661A3243G-PEO subject 317.937
GSM24662A3243G-PEO subject 422.237
GSM24663mtDNA "Common"-deletion subject 15153
GSM24664mtDNA "Common"-deletion subject 234.331
GSM24665mtDNA "Common"-deletion subject 332.535
GSM24666mtDNA "Common"-deletion subject 430.333