ProfileGDS1065 / 212506_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 83% 81% 87% 87% 87% 86% 87% 77% 81% 78% 82% 83% 90% 91% 90% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1223.383
GSM24653Normal subject 2177.281
GSM24654Normal subject 339587
GSM24655A3243G-MELAS subject 118787
GSM24656A3243G-MELAS subject 2290.487
GSM24657A3243G-MELAS subject 3465.286
GSM24658A3243G-MELAS subject 4285.587
GSM24659A3243G-PEO subject 1107.577
GSM24660A3243G-PEO subject 217381
GSM24661A3243G-PEO subject 3108.778
GSM24662A3243G-PEO subject 4165.282
GSM24663mtDNA "Common"-deletion subject 1227.283
GSM24664mtDNA "Common"-deletion subject 2744.290
GSM24665mtDNA "Common"-deletion subject 3758.591
GSM24666mtDNA "Common"-deletion subject 4786.390