ProfileGDS1065 / 213785_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 49% 55% 39% 29% 54% 49% 46% 55% 38% 52% 39% 67% 68% 56% 61% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 142.249
GSM24653Normal subject 251.455
GSM24654Normal subject 332.439
GSM24655A3243G-MELAS subject 112.329
GSM24656A3243G-MELAS subject 255.454
GSM24657A3243G-MELAS subject 359.949
GSM24658A3243G-MELAS subject 432.646
GSM24659A3243G-PEO subject 145.255
GSM24660A3243G-PEO subject 225.238
GSM24661A3243G-PEO subject 333.852
GSM24662A3243G-PEO subject 423.639
GSM24663mtDNA "Common"-deletion subject 195.967
GSM24664mtDNA "Common"-deletion subject 2164.768
GSM24665mtDNA "Common"-deletion subject 383.656
GSM24666mtDNA "Common"-deletion subject 410761