Source: ANIMAL_MODELS

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22931
Gene Symbol: RAB18
RAB18
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		0.200 Biomarker MGD ENU mutagenesis identifies mice modeling Warburg Micro Syndrome with sensory axon degeneration caused by a deletion in Rab18. 25779931

2015
Entrez Id: 22931
Gene Symbol: RAB18
RAB18
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		0.200 Biomarker MGD A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton. 24764192

2014