ProfileGDS1065 / 208425_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 8% 15% 9% 5% 5% 7% 8% 8% 8% 9% 8% 13% 10% 7% 6% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.58
GSM24653Normal subject 26.115
GSM24654Normal subject 34.19
GSM24655A3243G-MELAS subject 12.35
GSM24656A3243G-MELAS subject 23.25
GSM24657A3243G-MELAS subject 33.97
GSM24658A3243G-MELAS subject 42.98
GSM24659A3243G-PEO subject 13.68
GSM24660A3243G-PEO subject 23.58
GSM24661A3243G-PEO subject 339
GSM24662A3243G-PEO subject 43.18
GSM24663mtDNA "Common"-deletion subject 15.513
GSM24664mtDNA "Common"-deletion subject 27.310
GSM24665mtDNA "Common"-deletion subject 34.57
GSM24666mtDNA "Common"-deletion subject 43.66