ProfileGDS1065 / 219982_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 76% 65% 66% 72% 73% 66% 59% 71% 75% 69% 72% 71% 71% 71% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1143.176
GSM24653Normal subject 277.165
GSM24654Normal subject 3107.866
GSM24655A3243G-MELAS subject 175.372
GSM24656A3243G-MELAS subject 2121.273
GSM24657A3243G-MELAS subject 3134.566
GSM24658A3243G-MELAS subject 456.859
GSM24659A3243G-PEO subject 184.971
GSM24660A3243G-PEO subject 211775
GSM24661A3243G-PEO subject 367.969
GSM24662A3243G-PEO subject 494.272
GSM24663mtDNA "Common"-deletion subject 1115.371
GSM24664mtDNA "Common"-deletion subject 2195.771
GSM24665mtDNA "Common"-deletion subject 3168.171
GSM24666mtDNA "Common"-deletion subject 414867