ProfileGDS1065 / 204107_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 12% 24% 36% 13% 45% 6% 40% 38% 13% 16% 28% 20% 14% 10% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.912
GSM24653Normal subject 211.424
GSM24654Normal subject 327.636
GSM24655A3243G-MELAS subject 14.713
GSM24656A3243G-MELAS subject 239.745
GSM24657A3243G-MELAS subject 33.76
GSM24658A3243G-MELAS subject 425.940
GSM24659A3243G-PEO subject 123.638
GSM24660A3243G-PEO subject 25.313
GSM24661A3243G-PEO subject 35.116
GSM24662A3243G-PEO subject 413.128
GSM24663mtDNA "Common"-deletion subject 18.620
GSM24664mtDNA "Common"-deletion subject 210.414
GSM24665mtDNA "Common"-deletion subject 36.110
GSM24666mtDNA "Common"-deletion subject 47.414