ProfileGDS1065 / 221620_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 92% 93% 93% 92% 91% 84% 91% 87% 89% 90% 88% 91% 92% 92% 87% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1557.592
GSM24653Normal subject 2586.593
GSM24654Normal subject 3828.393
GSM24655A3243G-MELAS subject 1316.392
GSM24656A3243G-MELAS subject 2429.391
GSM24657A3243G-MELAS subject 339484
GSM24658A3243G-MELAS subject 4462.991
GSM24659A3243G-PEO subject 1209.987
GSM24660A3243G-PEO subject 2307.389
GSM24661A3243G-PEO subject 3283.390
GSM24662A3243G-PEO subject 4275.688
GSM24663mtDNA "Common"-deletion subject 1463.491
GSM24664mtDNA "Common"-deletion subject 2919.692
GSM24665mtDNA "Common"-deletion subject 3914.192
GSM24666mtDNA "Common"-deletion subject 454387