ProfileGDS1065 / 214261_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 55% 32% 55% 54% 53% 48% 25% 53% 54% 46% 54% 61% 40% 37% 44% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 154.755
GSM24653Normal subject 219.632
GSM24654Normal subject 365.855
GSM24655A3243G-MELAS subject 13754
GSM24656A3243G-MELAS subject 25353
GSM24657A3243G-MELAS subject 35848
GSM24658A3243G-MELAS subject 410.625
GSM24659A3243G-PEO subject 141.353
GSM24660A3243G-PEO subject 248.854
GSM24661A3243G-PEO subject 326.846
GSM24662A3243G-PEO subject 443.854
GSM24663mtDNA "Common"-deletion subject 172.461
GSM24664mtDNA "Common"-deletion subject 251.140
GSM24665mtDNA "Common"-deletion subject 33637
GSM24666mtDNA "Common"-deletion subject 450.744