ProfileGDS1065 / 217732_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% 96% 96% 96% 96% 96% 95% 96% 95% 94% 95% 97% 96% 96% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1901.695
GSM24653Normal subject 21026.696
GSM24654Normal subject 3172296
GSM24655A3243G-MELAS subject 1687.596
GSM24656A3243G-MELAS subject 21235.396
GSM24657A3243G-MELAS subject 31871.296
GSM24658A3243G-MELAS subject 41043.896
GSM24659A3243G-PEO subject 1625.595
GSM24660A3243G-PEO subject 2885.696
GSM24661A3243G-PEO subject 3636.995
GSM24662A3243G-PEO subject 464294
GSM24663mtDNA "Common"-deletion subject 1903.795
GSM24664mtDNA "Common"-deletion subject 22278.497
GSM24665mtDNA "Common"-deletion subject 32030.596
GSM24666mtDNA "Common"-deletion subject 42297.196