ProfileGDS1065 / 201629_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 27% 13% 68% 9% 15% 15% 52% 19% 38% 11% 19% 36% 42% 70% 41% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 114.427
GSM24653Normal subject 25.313
GSM24654Normal subject 3120.468
GSM24655A3243G-MELAS subject 13.59
GSM24656A3243G-MELAS subject 27.215
GSM24657A3243G-MELAS subject 38.515
GSM24658A3243G-MELAS subject 44352
GSM24659A3243G-PEO subject 17.919
GSM24660A3243G-PEO subject 225.238
GSM24661A3243G-PEO subject 33.611
GSM24662A3243G-PEO subject 47.319
GSM24663mtDNA "Common"-deletion subject 123.336
GSM24664mtDNA "Common"-deletion subject 257.442
GSM24665mtDNA "Common"-deletion subject 3158.670
GSM24666mtDNA "Common"-deletion subject 44541