ProfileGDS1065 / 202228_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 89% 90% 92% 92% 92% 88% 89% 87% 89% 87% 82% 89% 93% 92% 92% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1385.289
GSM24653Normal subject 2386.390
GSM24654Normal subject 3659.492
GSM24655A3243G-MELAS subject 1299.692
GSM24656A3243G-MELAS subject 2528.892
GSM24657A3243G-MELAS subject 3545.688
GSM24658A3243G-MELAS subject 4358.889
GSM24659A3243G-PEO subject 1205.987
GSM24660A3243G-PEO subject 2331.989
GSM24661A3243G-PEO subject 3206.587
GSM24662A3243G-PEO subject 4172.482
GSM24663mtDNA "Common"-deletion subject 139689
GSM24664mtDNA "Common"-deletion subject 2994.193
GSM24665mtDNA "Common"-deletion subject 3925.992
GSM24666mtDNA "Common"-deletion subject 41007.992