Gene: TMEM87B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84910
Gene Symbol: TMEM87B
TMEM87B 		0.010 Biomarker group BEFREE Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations. 24694933 2014