ProfileGDS1065 / 211071_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 73% 89% 68% 95% 80% 87% 74% 81% 77% 77% 90% 84% 66% 72% 62% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1122.673
GSM24653Normal subject 2329.689
GSM24654Normal subject 3117.368
GSM24655A3243G-MELAS subject 1530.695
GSM24656A3243G-MELAS subject 218380
GSM24657A3243G-MELAS subject 3480.887
GSM24658A3243G-MELAS subject 4117.474
GSM24659A3243G-PEO subject 114281
GSM24660A3243G-PEO subject 2130.777
GSM24661A3243G-PEO subject 3100.377
GSM24662A3243G-PEO subject 4316.890
GSM24663mtDNA "Common"-deletion subject 1250.784
GSM24664mtDNA "Common"-deletion subject 2151.966
GSM24665mtDNA "Common"-deletion subject 3175.372
GSM24666mtDNA "Common"-deletion subject 4116.162