ProfileGDS1065 / 206907_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 41% 52% 33% 63% 48% 54% 38% 68% 54% 55% 44% 54% 46% 49% 60% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 130.941
GSM24653Normal subject 246.252
GSM24654Normal subject 324.433
GSM24655A3243G-MELAS subject 151.463
GSM24656A3243G-MELAS subject 243.748
GSM24657A3243G-MELAS subject 377.454
GSM24658A3243G-MELAS subject 422.838
GSM24659A3243G-PEO subject 172.668
GSM24660A3243G-PEO subject 248.854
GSM24661A3243G-PEO subject 338.855
GSM24662A3243G-PEO subject 429.144
GSM24663mtDNA "Common"-deletion subject 152.954
GSM24664mtDNA "Common"-deletion subject 268.546
GSM24665mtDNA "Common"-deletion subject 361.849
GSM24666mtDNA "Common"-deletion subject 4105.460