ProfileGDS1065 / 210296_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 83% 80% 89% 80% 84% 79% 81% 81% 83% 76% 74% 80% 84% 90% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1221.783
GSM24653Normal subject 2167.580
GSM24654Normal subject 349989
GSM24655A3243G-MELAS subject 1116.280
GSM24656A3243G-MELAS subject 2232.484
GSM24657A3243G-MELAS subject 3276.979
GSM24658A3243G-MELAS subject 418681
GSM24659A3243G-PEO subject 113981
GSM24660A3243G-PEO subject 2187.283
GSM24661A3243G-PEO subject 394.976
GSM24662A3243G-PEO subject 4104.974
GSM24663mtDNA "Common"-deletion subject 1188.980
GSM24664mtDNA "Common"-deletion subject 2405.784
GSM24665mtDNA "Common"-deletion subject 367890
GSM24666mtDNA "Common"-deletion subject 4501.786