ProfileGDS1065 / 219772_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 98% 99% 99% 99% 99% 98% 98% 98% 99% 99% 98% 99% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1411398
GSM24653Normal subject 25044.699
GSM24654Normal subject 3601599
GSM24655A3243G-MELAS subject 13401.799
GSM24656A3243G-MELAS subject 2427399
GSM24657A3243G-MELAS subject 34299.798
GSM24658A3243G-MELAS subject 43537.798
GSM24659A3243G-PEO subject 12655.398
GSM24660A3243G-PEO subject 23345.699
GSM24661A3243G-PEO subject 33521.699
GSM24662A3243G-PEO subject 43387.198
GSM24663mtDNA "Common"-deletion subject 14757.199
GSM24664mtDNA "Common"-deletion subject 26682.799
GSM24665mtDNA "Common"-deletion subject 38677.799
GSM24666mtDNA "Common"-deletion subject 46741.899