ProfileGDS1065 / 216888_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 17% 13% 29% 18% 13% 31% 36% 13% 26% 20% 46% 25% 9% 29% 47% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.417
GSM24653Normal subject 25.313
GSM24654Normal subject 318.829
GSM24655A3243G-MELAS subject 16.218
GSM24656A3243G-MELAS subject 26.313
GSM24657A3243G-MELAS subject 326.131
GSM24658A3243G-MELAS subject 421.336
GSM24659A3243G-PEO subject 15.513
GSM24660A3243G-PEO subject 212.926
GSM24661A3243G-PEO subject 36.420
GSM24662A3243G-PEO subject 432.646
GSM24663mtDNA "Common"-deletion subject 112.625
GSM24664mtDNA "Common"-deletion subject 27.19
GSM24665mtDNA "Common"-deletion subject 323.429
GSM24666mtDNA "Common"-deletion subject 457.747