Gene: DCAF17 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80067
Gene Symbol: DCAF17
DCAF17 		0.110 CausalMutation disease CLINVAR Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome. 26612766 2016
Entrez Id: 80067
Gene Symbol: DCAF17
DCAF17 		0.110 GeneticVariation disease LHGDN Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome. 19026396 2008
Entrez Id: 80067
Gene Symbol: DCAF17
DCAF17 		0.110 Biomarker disease HPO