Gene: SCRIB ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23513
Gene Symbol: SCRIB
SCRIB 		0.020 GeneticVariation disease BEFREE In addition, we demonstrated that the craniorachischisis mouse line-90 mutation I285K, also affected SCRIB subcellular localization. 23922697 2013
Entrez Id: 23513
Gene Symbol: SCRIB
SCRIB 		0.020 GeneticVariation disease BEFREE We conclude that missense variants in CELSR1 and SCRIB may represent a cause of CRN in humans, as in mice, with defective PCP protein trafficking to the plasma membrane a likely pathogenic mechanism. 22095531 2012