ProfileGDS1065 / 211959_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 98% 99% 97% 97% 98% 98% 98% 98% 98% 98% 98% 97% 97% 98% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13279.998
GSM24653Normal subject 24128.599
GSM24654Normal subject 32077.197
GSM24655A3243G-MELAS subject 1858.397
GSM24656A3243G-MELAS subject 22813.198
GSM24657A3243G-MELAS subject 33555.198
GSM24658A3243G-MELAS subject 42350.698
GSM24659A3243G-PEO subject 12215.298
GSM24660A3243G-PEO subject 22146.598
GSM24661A3243G-PEO subject 32255.898
GSM24662A3243G-PEO subject 41917.798
GSM24663mtDNA "Common"-deletion subject 11564.497
GSM24664mtDNA "Common"-deletion subject 22447.297
GSM24665mtDNA "Common"-deletion subject 33737.898
GSM24666mtDNA "Common"-deletion subject 44701.398