ProfileGDS1065 / 208795_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 81% 81% 69% 81% 79% 77% 77% 83% 81% 85% 81% 81% 76% 77% 75% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1201.181
GSM24653Normal subject 2188.381
GSM24654Normal subject 3126.869
GSM24655A3243G-MELAS subject 1117.281
GSM24656A3243G-MELAS subject 2167.279
GSM24657A3243G-MELAS subject 324277
GSM24658A3243G-MELAS subject 4144.277
GSM24659A3243G-PEO subject 1154.983
GSM24660A3243G-PEO subject 216981
GSM24661A3243G-PEO subject 3167.885
GSM24662A3243G-PEO subject 4159.381
GSM24663mtDNA "Common"-deletion subject 120181
GSM24664mtDNA "Common"-deletion subject 2253.876
GSM24665mtDNA "Common"-deletion subject 3229.477
GSM24666mtDNA "Common"-deletion subject 4232.275