Gene: STPG4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 285051
Gene Symbol: STPG4
STPG4 		0.100 CausalMutation disease CLINVAR A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders. 26938784 2016
Entrez Id: 285051
Gene Symbol: STPG4
STPG4 		0.100 GeneticVariation disease CLINVAR Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease. 24417819 2014