ProfileGDS1065 / 211576_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 39% 37% 47% 41% 34% 46% 54% 60% 57% 53% 46% 59% 32% 43% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12839
GSM24653Normal subject 224.437
GSM24654Normal subject 345.647
GSM24655A3243G-MELAS subject 12341
GSM24656A3243G-MELAS subject 223.634
GSM24657A3243G-MELAS subject 352.646
GSM24658A3243G-MELAS subject 446.954
GSM24659A3243G-PEO subject 15560
GSM24660A3243G-PEO subject 253.757
GSM24661A3243G-PEO subject 334.953
GSM24662A3243G-PEO subject 432.146
GSM24663mtDNA "Common"-deletion subject 166.959
GSM24664mtDNA "Common"-deletion subject 235.232
GSM24665mtDNA "Common"-deletion subject 347.443
GSM24666mtDNA "Common"-deletion subject 413.721