Gene: ANKRD11 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11 		0.010 GeneticVariation group BEFREE Haploinsufficiency of ANKRD11 due to deletion or truncation mutations causes KBG syndrome, a rare genetic disorder characterized by intellectual disability, autism spectrum disorder, and craniofacial abnormalities. 29274743 2018