ProfileGDS1065 / 201819_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 59% 53% 59% 51% 70% 70% 59% 57% 52% 54% 64% 57% 55% 52% 55% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 163.959
GSM24653Normal subject 248.453
GSM24654Normal subject 377.359
GSM24655A3243G-MELAS subject 133.351
GSM24656A3243G-MELAS subject 2102.770
GSM24657A3243G-MELAS subject 3165.170
GSM24658A3243G-MELAS subject 457.159
GSM24659A3243G-PEO subject 148.857
GSM24660A3243G-PEO subject 245.352
GSM24661A3243G-PEO subject 33754
GSM24662A3243G-PEO subject 465.964
GSM24663mtDNA "Common"-deletion subject 161.157
GSM24664mtDNA "Common"-deletion subject 295.155
GSM24665mtDNA "Common"-deletion subject 370.952
GSM24666mtDNA "Common"-deletion subject 483.255