ProfileGDS1065 / 222199_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 67% 79% 62% 71% 66% 69% 65% 68% 68% 69% 72% 76% 69% 62% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 193.667
GSM24653Normal subject 2157.579
GSM24654Normal subject 389.162
GSM24655A3243G-MELAS subject 173.171
GSM24656A3243G-MELAS subject 28866
GSM24657A3243G-MELAS subject 3155.569
GSM24658A3243G-MELAS subject 477.265
GSM24659A3243G-PEO subject 172.868
GSM24660A3243G-PEO subject 28468
GSM24661A3243G-PEO subject 367.769
GSM24662A3243G-PEO subject 492.372
GSM24663mtDNA "Common"-deletion subject 1144.576
GSM24664mtDNA "Common"-deletion subject 2175.369
GSM24665mtDNA "Common"-deletion subject 3105.862
GSM24666mtDNA "Common"-deletion subject 4148.567