Gene: CLTC ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1213
Gene Symbol: CLTC
CLTC 		0.010 GeneticVariation disease BEFREE De novo CLTC variants are associated with a variable phenotype from mild to severe intellectual disability, microcephaly, hypoplasia of the corpus callosum, and epilepsy. 31776469 2019