ProfileGDS1065 / 211182_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 19% 17% 25% 47% 35% 18% 45% 8% 13% 17% 9% 15% 11% 17% 18% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.319
GSM24653Normal subject 27.117
GSM24654Normal subject 313.625
GSM24655A3243G-MELAS subject 12947
GSM24656A3243G-MELAS subject 22535
GSM24657A3243G-MELAS subject 310.618
GSM24658A3243G-MELAS subject 431.545
GSM24659A3243G-PEO subject 13.88
GSM24660A3243G-PEO subject 25.513
GSM24661A3243G-PEO subject 35.417
GSM24662A3243G-PEO subject 43.29
GSM24663mtDNA "Common"-deletion subject 16.315
GSM24664mtDNA "Common"-deletion subject 28.211
GSM24665mtDNA "Common"-deletion subject 31017
GSM24666mtDNA "Common"-deletion subject 410.618