ProfileGDS1065 / 220371_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% 64% 57% 74% 54% 56% 55% 64% 62% 69% 67% 64% 57% 45% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 193.467
GSM24653Normal subject 274.564
GSM24654Normal subject 371.857
GSM24655A3243G-MELAS subject 183.174
GSM24656A3243G-MELAS subject 256.154
GSM24657A3243G-MELAS subject 384.556
GSM24658A3243G-MELAS subject 449.355
GSM24659A3243G-PEO subject 162.364
GSM24660A3243G-PEO subject 266.162
GSM24661A3243G-PEO subject 368.469
GSM24662A3243G-PEO subject 474.267
GSM24663mtDNA "Common"-deletion subject 183.764
GSM24664mtDNA "Common"-deletion subject 2103.457
GSM24665mtDNA "Common"-deletion subject 35345
GSM24666mtDNA "Common"-deletion subject 498.159