ProfileGDS1065 / 204051_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 74% 89% 86% 82% 71% 72% 85% 83% 70% 83% 82% 66% 58% 81% 74% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 113174
GSM24653Normal subject 2354.789
GSM24654Normal subject 3343.886
GSM24655A3243G-MELAS subject 1126.582
GSM24656A3243G-MELAS subject 211271
GSM24657A3243G-MELAS subject 3182.672
GSM24658A3243G-MELAS subject 4233.985
GSM24659A3243G-PEO subject 1155.483
GSM24660A3243G-PEO subject 29370
GSM24661A3243G-PEO subject 3145.283
GSM24662A3243G-PEO subject 4166.282
GSM24663mtDNA "Common"-deletion subject 18966
GSM24664mtDNA "Common"-deletion subject 2106.958
GSM24665mtDNA "Common"-deletion subject 3294.481
GSM24666mtDNA "Common"-deletion subject 4214.974