ProfileGDS1065 / 218803_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 69% 72% 65% 78% 70% 74% 73% 77% 67% 76% 75% 80% 66% 75% 57% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1101.969
GSM24653Normal subject 2106.972
GSM24654Normal subject 3102.765
GSM24655A3243G-MELAS subject 1102.278
GSM24656A3243G-MELAS subject 2106.370
GSM24657A3243G-MELAS subject 3198.274
GSM24658A3243G-MELAS subject 4111.273
GSM24659A3243G-PEO subject 1108.977
GSM24660A3243G-PEO subject 280.767
GSM24661A3243G-PEO subject 396.376
GSM24662A3243G-PEO subject 4108.775
GSM24663mtDNA "Common"-deletion subject 1193.180
GSM24664mtDNA "Common"-deletion subject 2156.766
GSM24665mtDNA "Common"-deletion subject 3200.575
GSM24666mtDNA "Common"-deletion subject 492.357