RBM10, RNA binding motif protein 10, 8241

N. diseases: 99; N. variants: 8
Disease: Congenital Abnormality ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.010 GeneticVariation group BEFREE RBM10 encodes an RNA binding protein.Mutations in RBM10 are known to cause multiple congenital anomaly syndrome in male humans, the TARP syndrome. 24000153 2013