ProfileGDS1065 / 202273_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 71% 77% 71% 78% 69% 79% 82% 75% 71% 69% 77% 67% 72% 74% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1112.871
GSM24653Normal subject 2142.777
GSM24654Normal subject 3138.271
GSM24655A3243G-MELAS subject 199.978
GSM24656A3243G-MELAS subject 299.969
GSM24657A3243G-MELAS subject 3271.579
GSM24658A3243G-MELAS subject 4190.782
GSM24659A3243G-PEO subject 1100.375
GSM24660A3243G-PEO subject 297.371
GSM24661A3243G-PEO subject 370.569
GSM24662A3243G-PEO subject 4123.677
GSM24663mtDNA "Common"-deletion subject 19667
GSM24664mtDNA "Common"-deletion subject 2203.772
GSM24665mtDNA "Common"-deletion subject 3190.874
GSM24666mtDNA "Common"-deletion subject 4187.571