ProfileGDS1065 / 214359_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 90% 89% 96% 93% 95% 89% 93% 87% 92% 86% 82% 88% 95% 96% 92% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1438.290
GSM24653Normal subject 2349.989
GSM24654Normal subject 31363.396
GSM24655A3243G-MELAS subject 1374.193
GSM24656A3243G-MELAS subject 279695
GSM24657A3243G-MELAS subject 362589
GSM24658A3243G-MELAS subject 4611.993
GSM24659A3243G-PEO subject 1215.187
GSM24660A3243G-PEO subject 2452.192
GSM24661A3243G-PEO subject 317886
GSM24662A3243G-PEO subject 4162.882
GSM24663mtDNA "Common"-deletion subject 136588
GSM24664mtDNA "Common"-deletion subject 21454.795
GSM24665mtDNA "Common"-deletion subject 31716.796
GSM24666mtDNA "Common"-deletion subject 41016.192