ProfileGDS1065 / 215762_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 7% 22% 22% 24% 11% 10% 23% 26% 32% 12% 7% 21% 21% 21% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.47
GSM24653Normal subject 21022
GSM24654Normal subject 311.622
GSM24655A3243G-MELAS subject 19.324
GSM24656A3243G-MELAS subject 25.511
GSM24657A3243G-MELAS subject 35.510
GSM24658A3243G-MELAS subject 49.523
GSM24659A3243G-PEO subject 112.926
GSM24660A3243G-PEO subject 217.932
GSM24661A3243G-PEO subject 33.712
GSM24662A3243G-PEO subject 42.87
GSM24663mtDNA "Common"-deletion subject 19.321
GSM24664mtDNA "Common"-deletion subject 217.821
GSM24665mtDNA "Common"-deletion subject 313.821
GSM24666mtDNA "Common"-deletion subject 47.614