ProfileGDS1065 / 220745_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 26% 24% 25% 32% 31% 27% 25% 33% 27% 29% 39% 39% 52% 24% 28% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 113.926
GSM24653Normal subject 211.724
GSM24654Normal subject 313.725
GSM24655A3243G-MELAS subject 114.832
GSM24656A3243G-MELAS subject 220.731
GSM24657A3243G-MELAS subject 320.527
GSM24658A3243G-MELAS subject 410.425
GSM24659A3243G-PEO subject 118.233
GSM24660A3243G-PEO subject 214.127
GSM24661A3243G-PEO subject 311.129
GSM24662A3243G-PEO subject 42439
GSM24663mtDNA "Common"-deletion subject 127.339
GSM24664mtDNA "Common"-deletion subject 283.452
GSM24665mtDNA "Common"-deletion subject 317.524
GSM24666mtDNA "Common"-deletion subject 422.228