ProfileGDS1065 / 219657_s_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 64% 61% 57% 49% 56% 54% 56% 65% 64% 64% 50% 59% 58% 58% 50% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18064
GSM24653Normal subject 26661
GSM24654Normal subject 37257
GSM24655A3243G-MELAS subject 130.949
GSM24656A3243G-MELAS subject 259.856
GSM24657A3243G-MELAS subject 377.554
GSM24658A3243G-MELAS subject 450.156
GSM24659A3243G-PEO subject 166.465
GSM24660A3243G-PEO subject 271.164
GSM24661A3243G-PEO subject 356.164
GSM24662A3243G-PEO subject 436.950
GSM24663mtDNA "Common"-deletion subject 165.959
GSM24664mtDNA "Common"-deletion subject 2110.358
GSM24665mtDNA "Common"-deletion subject 390.258
GSM24666mtDNA "Common"-deletion subject 466.550