Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 282808
Gene Symbol: RAB40AL
RAB40AL 		0.600 Biomarker disease GENOMICS_ENGLAND Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. 26300074 2015
Entrez Id: 282808
Gene Symbol: RAB40AL
RAB40AL 		0.600 GeneticVariation disease UNIPROT Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder. 22581972 2012
Entrez Id: 282808
Gene Symbol: RAB40AL
RAB40AL 		0.600 Biomarker disease CTD_human Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder. 22581972 2012