Gene: MAB21L2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10586
Gene Symbol: MAB21L2
MAB21L2 		0.010 Biomarker group BEFREE In addition to the eye abnormality, patients with MAB21L2 <sup>R51C/+</sup> mutation also have skeletal dysplasia and intellectual disability. 30375740 2018