ProfileGDS1065 / 205706_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 16% 9% 16% 24% 22% 20% 12% 22% 24% 9% 7% 10% 32% 9% 40% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.716
GSM24653Normal subject 249
GSM24654Normal subject 37.616
GSM24655A3243G-MELAS subject 19.524
GSM24656A3243G-MELAS subject 211.922
GSM24657A3243G-MELAS subject 311.920
GSM24658A3243G-MELAS subject 4412
GSM24659A3243G-PEO subject 19.822
GSM24660A3243G-PEO subject 211.924
GSM24661A3243G-PEO subject 339
GSM24662A3243G-PEO subject 42.87
GSM24663mtDNA "Common"-deletion subject 14.310
GSM24664mtDNA "Common"-deletion subject 234.832
GSM24665mtDNA "Common"-deletion subject 35.29
GSM24666mtDNA "Common"-deletion subject 44340