Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23568
Gene Symbol: ARL2BP
ARL2BP
CUI: C4747737
Disease: RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS
RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS 		0.900 GeneticVariation UNIPROT ARL2BP mutations account for 0.1% of autosomal recessive rod-cone dystrophies with the report of a novel splice variant. 27790702

2017
Entrez Id: 23568
Gene Symbol: ARL2BP
ARL2BP
CUI: C4747737
Disease: RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS
RETINITIS PIGMENTOSA 82 WITH OR WITHOUT SITUS INVERSUS 		0.900 GeneticVariation UNIPROT Mutations in ARL2BP, encoding ADP-ribosylation-factor-like 2 binding protein, cause autosomal-recessive retinitis pigmentosa. 23849777

2013