Gene: KDM3B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51780
Gene Symbol: KDM3B
KDM3B 		0.310 Biomarker disease GENOMICS_ENGLAND De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism. 30929739 2019
Entrez Id: 51780
Gene Symbol: KDM3B
KDM3B 		0.310 GeneticVariation disease BEFREE By using exome sequencing and a gene matching approach, we identified de novo and inherited pathogenic variants in KDM3B in 14 unrelated individuals and three affected parents with varying degrees of intellectual disability (ID) or developmental delay (DD) and short stature. 30929739 2019