ProfileGDS1065 / 217361_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 22% 32% 24% 29% 36% 10% 47% 28% 14% 32% 34% 24% 12% 7% 18% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 110.122
GSM24653Normal subject 219.132
GSM24654Normal subject 313.124
GSM24655A3243G-MELAS subject 112.729
GSM24656A3243G-MELAS subject 226.336
GSM24657A3243G-MELAS subject 35.410
GSM24658A3243G-MELAS subject 434.847
GSM24659A3243G-PEO subject 114.428
GSM24660A3243G-PEO subject 26.114
GSM24661A3243G-PEO subject 313.732
GSM24662A3243G-PEO subject 418.634
GSM24663mtDNA "Common"-deletion subject 111.324
GSM24664mtDNA "Common"-deletion subject 29.212
GSM24665mtDNA "Common"-deletion subject 34.67
GSM24666mtDNA "Common"-deletion subject 41118