ProfileGDS1065 / 217020_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 70% 55% 62% 67% 62% 55% 57% 64% 60% 59% 62% 61% 67% 55% 49% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1106.170
GSM24653Normal subject 251.955
GSM24654Normal subject 389.762
GSM24655A3243G-MELAS subject 162.167
GSM24656A3243G-MELAS subject 275.862
GSM24657A3243G-MELAS subject 380.855
GSM24658A3243G-MELAS subject 452.957
GSM24659A3243G-PEO subject 16364
GSM24660A3243G-PEO subject 261.860
GSM24661A3243G-PEO subject 345.259
GSM24662A3243G-PEO subject 46062
GSM24663mtDNA "Common"-deletion subject 172.961
GSM24664mtDNA "Common"-deletion subject 2161.967
GSM24665mtDNA "Common"-deletion subject 381.455
GSM24666mtDNA "Common"-deletion subject 463.749