ProfileGDS1065 / 210191_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 38% 41% 46% 47% 38% 40% 36% 40% 37% 39% 43% 50% 40% 51% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 126.238
GSM24653Normal subject 229.141
GSM24654Normal subject 344.846
GSM24655A3243G-MELAS subject 128.947
GSM24656A3243G-MELAS subject 229.438
GSM24657A3243G-MELAS subject 341.640
GSM24658A3243G-MELAS subject 421.436
GSM24659A3243G-PEO subject 124.940
GSM24660A3243G-PEO subject 224.437
GSM24661A3243G-PEO subject 319.539
GSM24662A3243G-PEO subject 427.943
GSM24663mtDNA "Common"-deletion subject 145.450
GSM24664mtDNA "Common"-deletion subject 251.440
GSM24665mtDNA "Common"-deletion subject 367.551
GSM24666mtDNA "Common"-deletion subject 438.938