ProfileGDS1065 / 209984_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 61% 60% 66% 52% 55% 54% 61% 38% 55% 41% 33% 58% 64% 65% 54% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 171.561
GSM24653Normal subject 262.460
GSM24654Normal subject 3106.966
GSM24655A3243G-MELAS subject 134.452
GSM24656A3243G-MELAS subject 257.755
GSM24657A3243G-MELAS subject 377.654
GSM24658A3243G-MELAS subject 462.461
GSM24659A3243G-PEO subject 122.938
GSM24660A3243G-PEO subject 250.855
GSM24661A3243G-PEO subject 321.241
GSM24662A3243G-PEO subject 417.833
GSM24663mtDNA "Common"-deletion subject 162.458
GSM24664mtDNA "Common"-deletion subject 214464
GSM24665mtDNA "Common"-deletion subject 312265
GSM24666mtDNA "Common"-deletion subject 48054