ProfileGDS1065 / 204288_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 54% 70% 23% 52% 36% 73% 63% 43% 42% 21% 42% 20% 47% 53% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 153.254
GSM24653Normal subject 298.970
GSM24654Normal subject 312.423
GSM24655A3243G-MELAS subject 135.452
GSM24656A3243G-MELAS subject 225.836
GSM24657A3243G-MELAS subject 3191.373
GSM24658A3243G-MELAS subject 468.463
GSM24659A3243G-PEO subject 12943
GSM24660A3243G-PEO subject 230.142
GSM24661A3243G-PEO subject 36.721
GSM24662A3243G-PEO subject 427.442
GSM24663mtDNA "Common"-deletion subject 18.620
GSM24664mtDNA "Common"-deletion subject 27147
GSM24665mtDNA "Common"-deletion subject 374.153
GSM24666mtDNA "Common"-deletion subject 472.752