ProfileGDS1065 / 211383_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 83% 87% 85% 88% 88% 81% 84% 87% 86% 86% 87% 87% 85% 82% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1232.283
GSM24653Normal subject 229187
GSM24654Normal subject 3319.185
GSM24655A3243G-MELAS subject 1204.288
GSM24656A3243G-MELAS subject 2310.188
GSM24657A3243G-MELAS subject 3312.481
GSM24658A3243G-MELAS subject 4219.384
GSM24659A3243G-PEO subject 1201.287
GSM24660A3243G-PEO subject 2231.186
GSM24661A3243G-PEO subject 3191.486
GSM24662A3243G-PEO subject 4238.587
GSM24663mtDNA "Common"-deletion subject 1307.587
GSM24664mtDNA "Common"-deletion subject 2464.785
GSM24665mtDNA "Common"-deletion subject 3322.382
GSM24666mtDNA "Common"-deletion subject 4503.886