Gene: NEXMIF ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 340533
Gene Symbol: NEXMIF
NEXMIF 		0.020 GeneticVariation disease BEFREE KIAA2022 mutations and alterations have been reported in only four families with nonsyndromic ID and epilepsy. 25900396 2015
Entrez Id: 340533
Gene Symbol: NEXMIF
NEXMIF 		0.020 Biomarker disease BEFREE Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth. 23615299 2013