Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7 		0.710 GeneticVariation disease BEFREE Our findings expand the clinical and molecular spectrum of homozygous PRMT7 mutations, associated to the SBIDDS syndrome, showing a possible correlation between the type of mutation and the severity of the phenotype. 28902392 2018
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7 		0.710 Biomarker disease GENOMICS_ENGLAND Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly. 27718516 2017
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7 		0.710 GermlineCausalMutation disease ORPHANET Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families. 26437029 2015
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7 		0.710 GeneticVariation disease UNIPROT Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families. 26437029 2015
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7 		0.710 CausalMutation disease CLINVAR
Entrez Id: 54496
Gene Symbol: PRMT7
PRMT7 		0.710 GeneticVariation disease CLINVAR