ProfileGDS1065 / 201627_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 48% 61% 60% 61% 58% 60% 54% 55% 57% 64% 58% 56% 62% 69% 61% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 141.148
GSM24653Normal subject 264.661
GSM24654Normal subject 383.860
GSM24655A3243G-MELAS subject 148.461
GSM24656A3243G-MELAS subject 264.858
GSM24657A3243G-MELAS subject 399.960
GSM24658A3243G-MELAS subject 446.154
GSM24659A3243G-PEO subject 145.655
GSM24660A3243G-PEO subject 254.757
GSM24661A3243G-PEO subject 355.964
GSM24662A3243G-PEO subject 451.258
GSM24663mtDNA "Common"-deletion subject 158.856
GSM24664mtDNA "Common"-deletion subject 2131.962
GSM24665mtDNA "Common"-deletion subject 3146.869
GSM24666mtDNA "Common"-deletion subject 4110.661