ProfileGDS1065 / 214864_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 95% 96% 94% 96% 94% 95% 95% 96% 95% 96% 95% 96% 95% 95% 94% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1923.595
GSM24653Normal subject 2973.296
GSM24654Normal subject 3903.894
GSM24655A3243G-MELAS subject 1584.396
GSM24656A3243G-MELAS subject 2725.494
GSM24657A3243G-MELAS subject 31494.295
GSM24658A3243G-MELAS subject 481895
GSM24659A3243G-PEO subject 1785.396
GSM24660A3243G-PEO subject 2718.895
GSM24661A3243G-PEO subject 3700.996
GSM24662A3243G-PEO subject 4787.795
GSM24663mtDNA "Common"-deletion subject 11258.896
GSM24664mtDNA "Common"-deletion subject 2156695
GSM24665mtDNA "Common"-deletion subject 3147895
GSM24666mtDNA "Common"-deletion subject 4130994