ProfileGDS1065 / 206194_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 57% 56% 41% 73% 59% 75% 48% 50% 61% 62% 68% 51% 51% 51% 53% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 160.157
GSM24653Normal subject 255.156
GSM24654Normal subject 335.741
GSM24655A3243G-MELAS subject 180.273
GSM24656A3243G-MELAS subject 267.559
GSM24657A3243G-MELAS subject 3215.975
GSM24658A3243G-MELAS subject 436.648
GSM24659A3243G-PEO subject 137.250
GSM24660A3243G-PEO subject 262.361
GSM24661A3243G-PEO subject 351.862
GSM24662A3243G-PEO subject 477.668
GSM24663mtDNA "Common"-deletion subject 147.651
GSM24664mtDNA "Common"-deletion subject 280.651
GSM24665mtDNA "Common"-deletion subject 367.851
GSM24666mtDNA "Common"-deletion subject 476.553