ProfileGDS1065 / 210873_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 31% 8% 22% 24% 24% 4% 29% 26% 28% 6% 23% 32% 33% 30% 34% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11831
GSM24653Normal subject 23.78
GSM24654Normal subject 311.722
GSM24655A3243G-MELAS subject 19.324
GSM24656A3243G-MELAS subject 213.424
GSM24657A3243G-MELAS subject 32.84
GSM24658A3243G-MELAS subject 414.329
GSM24659A3243G-PEO subject 112.526
GSM24660A3243G-PEO subject 214.928
GSM24661A3243G-PEO subject 32.16
GSM24662A3243G-PEO subject 49.523
GSM24663mtDNA "Common"-deletion subject 118.832
GSM24664mtDNA "Common"-deletion subject 238.233
GSM24665mtDNA "Common"-deletion subject 325.230
GSM24666mtDNA "Common"-deletion subject 430.834