ProfileGDS1065 / 200099_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 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19969.599
GSM24653Normal subject 27539.199
GSM24654Normal subject 39796.999
GSM24655A3243G-MELAS subject 14359.199
GSM24656A3243G-MELAS subject 26167.399
GSM24657A3243G-MELAS subject 31075899
GSM24658A3243G-MELAS subject 48839.599
GSM24659A3243G-PEO subject 16032.399
GSM24660A3243G-PEO subject 26639.599
GSM24661A3243G-PEO subject 35546.899
GSM24662A3243G-PEO subject 47663.999
GSM24663mtDNA "Common"-deletion subject 18978.999
GSM24664mtDNA "Common"-deletion subject 210875.999
GSM24665mtDNA "Common"-deletion subject 310903.299
GSM24666mtDNA "Common"-deletion subject 412727.999