ProfileGDS1065 / 211107_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 64% 56% 59% 58% 42% 57% 54% 66% 48% 60% 53% 54% 61% 54% 55% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17964
GSM24653Normal subject 254.656
GSM24654Normal subject 379.759
GSM24655A3243G-MELAS subject 142.858
GSM24656A3243G-MELAS subject 235.142
GSM24657A3243G-MELAS subject 386.657
GSM24658A3243G-MELAS subject 446.554
GSM24659A3243G-PEO subject 166.866
GSM24660A3243G-PEO subject 238.148
GSM24661A3243G-PEO subject 346.760
GSM24662A3243G-PEO subject 441.553
GSM24663mtDNA "Common"-deletion subject 153.254
GSM24664mtDNA "Common"-deletion subject 2123.461
GSM24665mtDNA "Common"-deletion subject 377.154
GSM24666mtDNA "Common"-deletion subject 481.755