ProfileGDS1065 / 219458_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 61% 56% 55% 61% 58% 50% 44% 66% 65% 63% 62% 52% 47% 58% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 170.661
GSM24653Normal subject 253.756
GSM24654Normal subject 366.455
GSM24655A3243G-MELAS subject 14961
GSM24656A3243G-MELAS subject 265.558
GSM24657A3243G-MELAS subject 362.850
GSM24658A3243G-MELAS subject 430.344
GSM24659A3243G-PEO subject 168.866
GSM24660A3243G-PEO subject 274.765
GSM24661A3243G-PEO subject 353.263
GSM24662A3243G-PEO subject 461.462
GSM24663mtDNA "Common"-deletion subject 150.652
GSM24664mtDNA "Common"-deletion subject 270.747
GSM24665mtDNA "Common"-deletion subject 389.658
GSM24666mtDNA "Common"-deletion subject 496.658