Gene: RAB27A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5873
Gene Symbol: RAB27A
RAB27A 		0.020 GeneticVariation group BEFREE Human Griscelli syndrome type 2 (GS-2) is characterized by partial albinism and a severe immunologic disorder as a result of RAB27A mutations. 20370853 2010
Entrez Id: 5873
Gene Symbol: RAB27A
RAB27A 		0.020 GeneticVariation group BEFREE Mutations in the Rab27a gene cause pigment as well as cytotoxic granule transport defects, accounting for the partial albinism and severe immune disorder characteristics of this syndrome. 12446441 2003