ProfileGDS1065 / 219775_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 16% 42% 13% 24% 15% 23% 28% 35% 15% 20% 11% 40% 16% 10% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.816
GSM24653Normal subject 230.442
GSM24654Normal subject 35.813
GSM24655A3243G-MELAS subject 19.124
GSM24656A3243G-MELAS subject 27.215
GSM24657A3243G-MELAS subject 314.723
GSM24658A3243G-MELAS subject 412.928
GSM24659A3243G-PEO subject 119.835
GSM24660A3243G-PEO subject 26.615
GSM24661A3243G-PEO subject 36.620
GSM24662A3243G-PEO subject 4411
GSM24663mtDNA "Common"-deletion subject 12940
GSM24664mtDNA "Common"-deletion subject 211.916
GSM24665mtDNA "Common"-deletion subject 36.110
GSM24666mtDNA "Common"-deletion subject 47.514