ProfileGDS1065 / 205619_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 75% 64% 60% 78% 63% 76% 72% 60% 69% 74% 71% 77% 69% 68% 74% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1139.875
GSM24653Normal subject 276.664
GSM24654Normal subject 38260
GSM24655A3243G-MELAS subject 1100.678
GSM24656A3243G-MELAS subject 278.263
GSM24657A3243G-MELAS subject 3220.476
GSM24658A3243G-MELAS subject 4109.172
GSM24659A3243G-PEO subject 154.660
GSM24660A3243G-PEO subject 287.269
GSM24661A3243G-PEO subject 389.174
GSM24662A3243G-PEO subject 487.871
GSM24663mtDNA "Common"-deletion subject 1156.177
GSM24664mtDNA "Common"-deletion subject 2176.369
GSM24665mtDNA "Common"-deletion subject 3145.668
GSM24666mtDNA "Common"-deletion subject 4217.974