ProfileGDS1065 / 202095_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 55% 59% 36% 66% 44% 45% 50% 67% 51% 61% 49% 51% 33% 43% 39% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 154.455
GSM24653Normal subject 261.559
GSM24654Normal subject 327.736
GSM24655A3243G-MELAS subject 157.566
GSM24656A3243G-MELAS subject 23844
GSM24657A3243G-MELAS subject 350.745
GSM24658A3243G-MELAS subject 439.850
GSM24659A3243G-PEO subject 169.767
GSM24660A3243G-PEO subject 242.751
GSM24661A3243G-PEO subject 349.161
GSM24662A3243G-PEO subject 436.249
GSM24663mtDNA "Common"-deletion subject 146.551
GSM24664mtDNA "Common"-deletion subject 238.133
GSM24665mtDNA "Common"-deletion subject 349.543
GSM24666mtDNA "Common"-deletion subject 441.239