ProfileGDS1065 / 216438_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 97% 98% 96% 98% 97% 98% 98% 97% 97% 98% 98% 96% 97% 97% 97% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12014.897
GSM24653Normal subject 22853.798
GSM24654Normal subject 31754.296
GSM24655A3243G-MELAS subject 11254.998
GSM24656A3243G-MELAS subject 21800.297
GSM24657A3243G-MELAS subject 3412698
GSM24658A3243G-MELAS subject 42427.898
GSM24659A3243G-PEO subject 11428.997
GSM24660A3243G-PEO subject 21489.697
GSM24661A3243G-PEO subject 31448.898
GSM24662A3243G-PEO subject 41827.998
GSM24663mtDNA "Common"-deletion subject 11425.696
GSM24664mtDNA "Common"-deletion subject 23030.797
GSM24665mtDNA "Common"-deletion subject 32888.797
GSM24666mtDNA "Common"-deletion subject 43440.197