ProfileGDS1065 / 203349_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 70% 81% 78% 83% 57% 75% 77% 86% 70% 78% 76% 83% 73% 59% 61% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1106.870
GSM24653Normal subject 2176.281
GSM24654Normal subject 3204.578
GSM24655A3243G-MELAS subject 1133.483
GSM24656A3243G-MELAS subject 262.757
GSM24657A3243G-MELAS subject 3211.975
GSM24658A3243G-MELAS subject 4139.777
GSM24659A3243G-PEO subject 119686
GSM24660A3243G-PEO subject 292.170
GSM24661A3243G-PEO subject 310878
GSM24662A3243G-PEO subject 4119.376
GSM24663mtDNA "Common"-deletion subject 123983
GSM24664mtDNA "Common"-deletion subject 2213.273
GSM24665mtDNA "Common"-deletion subject 395.259
GSM24666mtDNA "Common"-deletion subject 4106.761