RANBP1, RAN binding protein 1, 5902

N. diseases: 18; N. variants: 0
Disease: Emanuel syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1836929
Disease: Emanuel syndrome
Emanuel syndrome 		0.010 GeneticVariation disease BEFREE Hamster-human somatic hybrid cell lines from a patient with der(22) syndrome and a patient with VCFS showed that the breakpoints occurred in an interval containing low-copy repeats, distal to RANBP1 and proximal to ZNF74. 10053009 1999