ProfileGDS1065 / 212300_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 43% 20% 55% 36% 16% 57% 56% 58% 58% 52% 53% 19% 52% 56% 49% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 133.643
GSM24653Normal subject 2920
GSM24654Normal subject 366.455
GSM24655A3243G-MELAS subject 118.536
GSM24656A3243G-MELAS subject 27.616
GSM24657A3243G-MELAS subject 38857
GSM24658A3243G-MELAS subject 45056
GSM24659A3243G-PEO subject 150.458
GSM24660A3243G-PEO subject 256.158
GSM24661A3243G-PEO subject 334.352
GSM24662A3243G-PEO subject 441.853
GSM24663mtDNA "Common"-deletion subject 18.419
GSM24664mtDNA "Common"-deletion subject 283.852
GSM24665mtDNA "Common"-deletion subject 384.856
GSM24666mtDNA "Common"-deletion subject 464.349