ProfileGDS1065 / 201119_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 17387.499
GSM24653Normal subject 26646.799
GSM24654Normal subject 37140.199
GSM24655A3243G-MELAS subject 13135.599
GSM24656A3243G-MELAS subject 24432.599
GSM24657A3243G-MELAS subject 37543.999
GSM24658A3243G-MELAS subject 45801.799
GSM24659A3243G-PEO subject 14248.799
GSM24660A3243G-PEO subject 24907.599
GSM24661A3243G-PEO subject 34485.399
GSM24662A3243G-PEO subject 46016.899
GSM24663mtDNA "Common"-deletion subject 16475.199
GSM24664mtDNA "Common"-deletion subject 27064.999
GSM24665mtDNA "Common"-deletion subject 37733.599
GSM24666mtDNA "Common"-deletion subject 48506.599