ProfileGDS1065 / 207642_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 44% 38% 45% 46% 43% 38% 40% 50% 47% 52% 43% 46% 43% 46% 37% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 134.244
GSM24653Normal subject 226.138
GSM24654Normal subject 343.345
GSM24655A3243G-MELAS subject 127.546
GSM24656A3243G-MELAS subject 235.743
GSM24657A3243G-MELAS subject 336.438
GSM24658A3243G-MELAS subject 425.540
GSM24659A3243G-PEO subject 13850
GSM24660A3243G-PEO subject 236.647
GSM24661A3243G-PEO subject 334.552
GSM24662A3243G-PEO subject 428.243
GSM24663mtDNA "Common"-deletion subject 137.946
GSM24664mtDNA "Common"-deletion subject 259.443
GSM24665mtDNA "Common"-deletion subject 356.146
GSM24666mtDNA "Common"-deletion subject 436.637