ProfileGDS1065 / 219989_s_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 27% 6% 8% 8% 6% 8% 8% 24% 26% 9% 8% 6% 10% 7% 8% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 114.627
GSM24653Normal subject 236
GSM24654Normal subject 33.88
GSM24655A3243G-MELAS subject 138
GSM24656A3243G-MELAS subject 23.36
GSM24657A3243G-MELAS subject 34.58
GSM24658A3243G-MELAS subject 42.88
GSM24659A3243G-PEO subject 111.324
GSM24660A3243G-PEO subject 21326
GSM24661A3243G-PEO subject 339
GSM24662A3243G-PEO subject 42.98
GSM24663mtDNA "Common"-deletion subject 12.96
GSM24664mtDNA "Common"-deletion subject 27.410
GSM24665mtDNA "Common"-deletion subject 34.77
GSM24666mtDNA "Common"-deletion subject 44.68