Gene: SPTAN1 ×
Source: INFERRED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		0.120 CausalMutation phenotype CLINVAR SPTAN1 encephalopathy: distinct phenotypes and genotypes. 25631096 2015
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		0.120 CausalMutation phenotype CLINVAR Progressive diffuse brain atrophy in West syndrome with marked hypomyelination due to SPTAN1 gene mutation. 22656320 2013
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		0.120 Biomarker phenotype HPO