ProfileGDS1065 / 37232_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 41% 48% 40% 43% 44% 50% 44% 51% 49% 36% 48% 47% 45% 40% 53% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 130.441
GSM24653Normal subject 238.748
GSM24654Normal subject 334.340
GSM24655A3243G-MELAS subject 124.443
GSM24656A3243G-MELAS subject 237.844
GSM24657A3243G-MELAS subject 364.350
GSM24658A3243G-MELAS subject 430.144
GSM24659A3243G-PEO subject 138.851
GSM24660A3243G-PEO subject 239.149
GSM24661A3243G-PEO subject 316.636
GSM24662A3243G-PEO subject 43548
GSM24663mtDNA "Common"-deletion subject 14147
GSM24664mtDNA "Common"-deletion subject 263.645
GSM24665mtDNA "Common"-deletion subject 34240
GSM24666mtDNA "Common"-deletion subject 475.853