ProfileGDS1065 / 216955_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 65% 61% 61% 63% 65% 61% 59% 61% 65% 72% 59% 67% 60% 66% 61% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18365
GSM24653Normal subject 265.361
GSM24654Normal subject 387.561
GSM24655A3243G-MELAS subject 152.663
GSM24656A3243G-MELAS subject 282.665
GSM24657A3243G-MELAS subject 3107.361
GSM24658A3243G-MELAS subject 458.959
GSM24659A3243G-PEO subject 157.361
GSM24660A3243G-PEO subject 275.565
GSM24661A3243G-PEO subject 379.672
GSM24662A3243G-PEO subject 453.659
GSM24663mtDNA "Common"-deletion subject 192.567
GSM24664mtDNA "Common"-deletion subject 2119.560
GSM24665mtDNA "Common"-deletion subject 312666
GSM24666mtDNA "Common"-deletion subject 4108.661