ProfileGDS1065 / 213830_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 20% 19% 17% 15% 23% 22% 20% 24% 24% 26% 25% 26% 17% 24% 22% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.120
GSM24653Normal subject 2819
GSM24654Normal subject 38.117
GSM24655A3243G-MELAS subject 15.115
GSM24656A3243G-MELAS subject 212.123
GSM24657A3243G-MELAS subject 313.822
GSM24658A3243G-MELAS subject 47.720
GSM24659A3243G-PEO subject 111.124
GSM24660A3243G-PEO subject 211.724
GSM24661A3243G-PEO subject 39.126
GSM24662A3243G-PEO subject 411.125
GSM24663mtDNA "Common"-deletion subject 113.326
GSM24664mtDNA "Common"-deletion subject 213.417
GSM24665mtDNA "Common"-deletion subject 316.824
GSM24666mtDNA "Common"-deletion subject 414.422