ProfileGDS1065 / 202289_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 97% 97% 96% 97% 98% 98% 98% 98% 98% 97% 98% 98% 98% 97% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1205397
GSM24653Normal subject 22011.997
GSM24654Normal subject 31745.196
GSM24655A3243G-MELAS subject 195797
GSM24656A3243G-MELAS subject 22131.798
GSM24657A3243G-MELAS subject 34389.298
GSM24658A3243G-MELAS subject 42060.998
GSM24659A3243G-PEO subject 11658.398
GSM24660A3243G-PEO subject 21942.798
GSM24661A3243G-PEO subject 3138997
GSM24662A3243G-PEO subject 42361.898
GSM24663mtDNA "Common"-deletion subject 12683.798
GSM24664mtDNA "Common"-deletion subject 23586.398
GSM24665mtDNA "Common"-deletion subject 32727.697
GSM24666mtDNA "Common"-deletion subject 44140.198