ProfileGDS1065 / 202687_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 40% 56% 62% 54% 49% 46% 70% 47% 50% 42% 35% 42% 69% 67% 57% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 128.940
GSM24653Normal subject 254.656
GSM24654Normal subject 388.462
GSM24655A3243G-MELAS subject 137.154
GSM24656A3243G-MELAS subject 24549
GSM24657A3243G-MELAS subject 354.646
GSM24658A3243G-MELAS subject 497.570
GSM24659A3243G-PEO subject 134.347
GSM24660A3243G-PEO subject 241.950
GSM24661A3243G-PEO subject 322.342
GSM24662A3243G-PEO subject 420.335
GSM24663mtDNA "Common"-deletion subject 131.642
GSM24664mtDNA "Common"-deletion subject 2177.369
GSM24665mtDNA "Common"-deletion subject 3137.967
GSM24666mtDNA "Common"-deletion subject 492.357