ProfileGDS1065 / 201317_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 95% 95% 96% 95% 96% 96% 95% 95% 96% 94% 95% 95% 96% 97% 96% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11048.495
GSM24653Normal subject 2886.795
GSM24654Normal subject 31759.296
GSM24655A3243G-MELAS subject 1549.595
GSM24656A3243G-MELAS subject 2116296
GSM24657A3243G-MELAS subject 31931.296
GSM24658A3243G-MELAS subject 4904.395
GSM24659A3243G-PEO subject 1557.395
GSM24660A3243G-PEO subject 2896.796
GSM24661A3243G-PEO subject 3524.894
GSM24662A3243G-PEO subject 4668.495
GSM24663mtDNA "Common"-deletion subject 1996.495
GSM24664mtDNA "Common"-deletion subject 22076.796
GSM24665mtDNA "Common"-deletion subject 32325.897
GSM24666mtDNA "Common"-deletion subject 42370.296