Gene: ARL6IP6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 151188
Gene Symbol: ARL6IP6
ARL6IP6 		0.010 GeneticVariation disease BEFREE We have identified a homozygous truncating mutation in ARL6IP6 as the likely cause of a syndromic form of CMTC associated with major dysmorphism, developmental delay, transient ischemic attacks and cerebral vascular malformations. 25957586 2015