ProfileGDS1065 / 213530_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 70% 57% 69% 49% 67% 73% 65% 54% 62% 47% 63% 69% 37% 72% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1102.970
GSM24653Normal subject 256.857
GSM24654Normal subject 3122.269
GSM24655A3243G-MELAS subject 131.849
GSM24656A3243G-MELAS subject 293.167
GSM24657A3243G-MELAS subject 3185.273
GSM24658A3243G-MELAS subject 476.365
GSM24659A3243G-PEO subject 143.654
GSM24660A3243G-PEO subject 265.762
GSM24661A3243G-PEO subject 328.447
GSM24662A3243G-PEO subject 462.963
GSM24663mtDNA "Common"-deletion subject 1105.369
GSM24664mtDNA "Common"-deletion subject 244.937
GSM24665mtDNA "Common"-deletion subject 3172.272
GSM24666mtDNA "Common"-deletion subject 4205.473