ProfileGDS1065 / 220243_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 10% 18% 16% 20% 20% 9% 8% 18% 14% 17% 13% 9% 19% 21% 13% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.310
GSM24653Normal subject 27.418
GSM24654Normal subject 37.416
GSM24655A3243G-MELAS subject 17.120
GSM24656A3243G-MELAS subject 29.920
GSM24657A3243G-MELAS subject 34.99
GSM24658A3243G-MELAS subject 42.88
GSM24659A3243G-PEO subject 17.418
GSM24660A3243G-PEO subject 25.914
GSM24661A3243G-PEO subject 35.217
GSM24662A3243G-PEO subject 44.613
GSM24663mtDNA "Common"-deletion subject 13.89
GSM24664mtDNA "Common"-deletion subject 21519
GSM24665mtDNA "Common"-deletion subject 313.321
GSM24666mtDNA "Common"-deletion subject 47.113