Gene: RBM28 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55131
Gene Symbol: RBM28
RBM28 		0.110 GeneticVariation disease BEFREE A homozygous loss-of-function mutation in the gene RBM28 was recently reported to underlie alopecia, neurological defects, and endocrinopathy (ANE) syndrome. 20231366 2010
Entrez Id: 55131
Gene Symbol: RBM28
RBM28 		0.110 Biomarker disease HPO