ProfileGDS1065 / 216925_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 30% 30% 22% 48% 44% 55% 40% 45% 46% 46% 55% 35% 29% 33% 17% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 117.130
GSM24653Normal subject 21730
GSM24654Normal subject 311.722
GSM24655A3243G-MELAS subject 130.248
GSM24656A3243G-MELAS subject 237.944
GSM24657A3243G-MELAS subject 380.855
GSM24658A3243G-MELAS subject 425.640
GSM24659A3243G-PEO subject 131.845
GSM24660A3243G-PEO subject 235.846
GSM24661A3243G-PEO subject 326.146
GSM24662A3243G-PEO subject 445.955
GSM24663mtDNA "Common"-deletion subject 122.435
GSM24664mtDNA "Common"-deletion subject 229.129
GSM24665mtDNA "Common"-deletion subject 330.433
GSM24666mtDNA "Common"-deletion subject 49.617