ProfileGDS1065 / 212014_x_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 71% 55% 56% 75% 77% 63% 73% 61% 70% 76% 66% 65% 50% 71% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1111.571
GSM24653Normal subject 252.855
GSM24654Normal subject 369.956
GSM24655A3243G-MELAS subject 18775
GSM24656A3243G-MELAS subject 2147.977
GSM24657A3243G-MELAS subject 3114.263
GSM24658A3243G-MELAS subject 4112.573
GSM24659A3243G-PEO subject 157.261
GSM24660A3243G-PEO subject 290.670
GSM24661A3243G-PEO subject 396.676
GSM24662A3243G-PEO subject 470.566
GSM24663mtDNA "Common"-deletion subject 186.865
GSM24664mtDNA "Common"-deletion subject 279.250
GSM24665mtDNA "Common"-deletion subject 3162.571
GSM24666mtDNA "Common"-deletion subject 473.152