ProfileGDS1065 / 206628_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 52% 57% 60% 56% 49% 47% 51% 62% 57% 57% 55% 55% 49% 57% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 149.152
GSM24653Normal subject 256.757
GSM24654Normal subject 382.360
GSM24655A3243G-MELAS subject 140.256
GSM24656A3243G-MELAS subject 244.949
GSM24657A3243G-MELAS subject 356.647
GSM24658A3243G-MELAS subject 441.651
GSM24659A3243G-PEO subject 158.962
GSM24660A3243G-PEO subject 254.357
GSM24661A3243G-PEO subject 341.657
GSM24662A3243G-PEO subject 445.455
GSM24663mtDNA "Common"-deletion subject 155.555
GSM24664mtDNA "Common"-deletion subject 274.949
GSM24665mtDNA "Common"-deletion subject 388.657
GSM24666mtDNA "Common"-deletion subject 473.852