ProfileGDS1065 / 218333_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 58% 61% 62% 40% 29% 70% 64% 56% 48% 53% 45% 51% 57% 58% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 162.658
GSM24653Normal subject 266.461
GSM24654Normal subject 389.162
GSM24655A3243G-MELAS subject 121.940
GSM24656A3243G-MELAS subject 218.829
GSM24657A3243G-MELAS subject 3158.870
GSM24658A3243G-MELAS subject 47364
GSM24659A3243G-PEO subject 146.556
GSM24660A3243G-PEO subject 238.948
GSM24661A3243G-PEO subject 335.953
GSM24662A3243G-PEO subject 430.445
GSM24663mtDNA "Common"-deletion subject 146.551
GSM24664mtDNA "Common"-deletion subject 2106.257
GSM24665mtDNA "Common"-deletion subject 392.258
GSM24666mtDNA "Common"-deletion subject 4144.867