ProfileGDS1065 / 209153_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 59% 66% 50% 15% 55% 61% 58% 57% 34% 59% 53% 65% 61% 50% 48% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 165.359
GSM24653Normal subject 282.666
GSM24654Normal subject 353.950
GSM24655A3243G-MELAS subject 15.115
GSM24656A3243G-MELAS subject 256.855
GSM24657A3243G-MELAS subject 3106.561
GSM24658A3243G-MELAS subject 454.458
GSM24659A3243G-PEO subject 148.857
GSM24660A3243G-PEO subject 220.234
GSM24661A3243G-PEO subject 34559
GSM24662A3243G-PEO subject 441.853
GSM24663mtDNA "Common"-deletion subject 184.365
GSM24664mtDNA "Common"-deletion subject 2122.161
GSM24665mtDNA "Common"-deletion subject 365.250
GSM24666mtDNA "Common"-deletion subject 461.748