ProfileGDS1065 / 205761_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% 38% 56% 63% 39% 48% 44% 12% 40% 52% 37% 50% 52% 49% 47% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 126.638
GSM24653Normal subject 225.738
GSM24654Normal subject 369.456
GSM24655A3243G-MELAS subject 151.263
GSM24656A3243G-MELAS subject 229.939
GSM24657A3243G-MELAS subject 359.248
GSM24658A3243G-MELAS subject 430.644
GSM24659A3243G-PEO subject 14.912
GSM24660A3243G-PEO subject 227.940
GSM24661A3243G-PEO subject 334.252
GSM24662A3243G-PEO subject 421.637
GSM24663mtDNA "Common"-deletion subject 146.450
GSM24664mtDNA "Common"-deletion subject 284.652
GSM24665mtDNA "Common"-deletion subject 361.549
GSM24666mtDNA "Common"-deletion subject 457.947