Gene: VANGL1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 81839
Gene Symbol: VANGL1
VANGL1 		0.110 Biomarker disease BEFREE PCP rare putative mutations had a weaker role in myelomeningocele (SB), being found in approximately 6% of cases and cumulated across CELSR1, FUZ, FZD6, PRICKLE1, VANGL1, and VANGL2. 23024041 2012
Entrez Id: 81839
Gene Symbol: VANGL1
VANGL1 		0.110 Biomarker disease HPO