ProfileGDS1065 / 221551_x_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 50% 51% 51% 64% 55% 57% 58% 55% 58% 62% 55% 46% 59% 49% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 144.650
GSM24653Normal subject 24451
GSM24654Normal subject 35551
GSM24655A3243G-MELAS subject 153.364
GSM24656A3243G-MELAS subject 25855
GSM24657A3243G-MELAS subject 388.157
GSM24658A3243G-MELAS subject 455.458
GSM24659A3243G-PEO subject 145.155
GSM24660A3243G-PEO subject 256.258
GSM24661A3243G-PEO subject 350.962
GSM24662A3243G-PEO subject 446.255
GSM24663mtDNA "Common"-deletion subject 139.246
GSM24664mtDNA "Common"-deletion subject 2112.459
GSM24665mtDNA "Common"-deletion subject 361.649
GSM24666mtDNA "Common"-deletion subject 448.643