ProfileGDS1065 / 208158_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 95% 94% 94% 91% 94% 96% 96% 94% 95% 96% 93% 94% 94% 95% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11061.895
GSM24653Normal subject 2704.594
GSM24654Normal subject 3973.794
GSM24655A3243G-MELAS subject 1284.591
GSM24656A3243G-MELAS subject 2749.994
GSM24657A3243G-MELAS subject 31792.996
GSM24658A3243G-MELAS subject 4112896
GSM24659A3243G-PEO subject 1447.194
GSM24660A3243G-PEO subject 2713.895
GSM24661A3243G-PEO subject 3678.196
GSM24662A3243G-PEO subject 4538.293
GSM24663mtDNA "Common"-deletion subject 1752.694
GSM24664mtDNA "Common"-deletion subject 21191.894
GSM24665mtDNA "Common"-deletion subject 31382.395
GSM24666mtDNA "Common"-deletion subject 4177495