ProfileGDS1065 / 217448_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 34% 32% 42% 25% 38% 33% 33% 18% 24% 25% 26% 32% 33% 17% 29% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 121.834
GSM24653Normal subject 218.932
GSM24654Normal subject 336.342
GSM24655A3243G-MELAS subject 11025
GSM24656A3243G-MELAS subject 229.338
GSM24657A3243G-MELAS subject 328.633
GSM24658A3243G-MELAS subject 417.733
GSM24659A3243G-PEO subject 17.418
GSM24660A3243G-PEO subject 211.424
GSM24661A3243G-PEO subject 38.925
GSM24662A3243G-PEO subject 411.526
GSM24663mtDNA "Common"-deletion subject 119.232
GSM24664mtDNA "Common"-deletion subject 236.933
GSM24665mtDNA "Common"-deletion subject 310.417
GSM24666mtDNA "Common"-deletion subject 423.329