ProfileGDS1065 / 207534_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 2% 24% 3% 2% 4% 21% 2% 11% 3% 7% 22% 3% 15% 15% 12% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11.82
GSM24653Normal subject 211.324
GSM24654Normal subject 32.23
GSM24655A3243G-MELAS subject 11.22
GSM24656A3243G-MELAS subject 22.64
GSM24657A3243G-MELAS subject 313.321
GSM24658A3243G-MELAS subject 41.32
GSM24659A3243G-PEO subject 14.611
GSM24660A3243G-PEO subject 22.13
GSM24661A3243G-PEO subject 32.37
GSM24662A3243G-PEO subject 48.722
GSM24663mtDNA "Common"-deletion subject 12.13
GSM24664mtDNA "Common"-deletion subject 211.115
GSM24665mtDNA "Common"-deletion subject 39.115
GSM24666mtDNA "Common"-deletion subject 46.412