Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 116442
Gene Symbol: RAB39B
RAB39B
0.410 GeneticVariation disease BEFREE Mutations in the RAB39B gene cause intellectual disability comorbid with autism spectrum disorder and epilepsy, but the impact of RAB39B loss of function on synaptic activity is largely unexplained. 25784538 2015
Entrez Id: 116442
Gene Symbol: RAB39B
RAB39B
0.410 Biomarker disease CTD_human Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly. 20159109 2010
Entrez Id: 116442
Gene Symbol: RAB39B
RAB39B
0.410 Biomarker disease HPO