ProfileGDS1065 / 213392_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 66% 60% 68% 69% 73% 68% 64% 59% 62% 70% 69% 65% 64% 69% 64% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 187.966
GSM24653Normal subject 264.160
GSM24654Normal subject 3117.268
GSM24655A3243G-MELAS subject 167.369
GSM24656A3243G-MELAS subject 2119.573
GSM24657A3243G-MELAS subject 3148.268
GSM24658A3243G-MELAS subject 471.264
GSM24659A3243G-PEO subject 153.359
GSM24660A3243G-PEO subject 266.462
GSM24661A3243G-PEO subject 372.170
GSM24662A3243G-PEO subject 481.269
GSM24663mtDNA "Common"-deletion subject 186.565
GSM24664mtDNA "Common"-deletion subject 2141.364
GSM24665mtDNA "Common"-deletion subject 315369
GSM24666mtDNA "Common"-deletion subject 4127.764