ProfileGDS1065 / 213892_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 73% 75% 73% 73% 71% 80% 75% 81% 77% 81% 82% 82% 74% 69% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1122.673
GSM24653Normal subject 2128.175
GSM24654Normal subject 3150.673
GSM24655A3243G-MELAS subject 179.673
GSM24656A3243G-MELAS subject 2107.771
GSM24657A3243G-MELAS subject 3297.680
GSM24658A3243G-MELAS subject 4128.475
GSM24659A3243G-PEO subject 1136.781
GSM24660A3243G-PEO subject 2130.377
GSM24661A3243G-PEO subject 3132.881
GSM24662A3243G-PEO subject 4172.282
GSM24663mtDNA "Common"-deletion subject 1209.482
GSM24664mtDNA "Common"-deletion subject 2228.974
GSM24665mtDNA "Common"-deletion subject 3149.569
GSM24666mtDNA "Common"-deletion subject 4174.770