Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54221
Gene Symbol: SNTG2
SNTG2
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.310 Biomarker CTD_human Interestingly, the binding was influenced by autism-related mutations, implying that the impaired interaction between NLs and SNTG2 contributes to the etiology of autism. 17292328

2007