ProfileGDS1065 / 202545_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 10% 12% 8% 21% 21% 5% 24% 11% 12% 14% 8% 11% 8% 21% 4% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.110
GSM24653Normal subject 2512
GSM24654Normal subject 33.78
GSM24655A3243G-MELAS subject 17.821
GSM24656A3243G-MELAS subject 210.821
GSM24657A3243G-MELAS subject 335
GSM24658A3243G-MELAS subject 49.724
GSM24659A3243G-PEO subject 14.711
GSM24660A3243G-PEO subject 25.212
GSM24661A3243G-PEO subject 34.414
GSM24662A3243G-PEO subject 438
GSM24663mtDNA "Common"-deletion subject 14.711
GSM24664mtDNA "Common"-deletion subject 26.38
GSM24665mtDNA "Common"-deletion subject 313.421
GSM24666mtDNA "Common"-deletion subject 42.74