LAMB1, laminin subunit beta 1, 3912

N. diseases: 75; N. variants: 14
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 GeneticVariation disease BEFREE LAMB1 polymorphism is associated with autism symptom severity in Korean autism spectrum disorder patients. 25774865 2015
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 Biomarker disease CTD_human Analysis of genetic variants provided evidence for association with autism for one of the new missense changes identified in LAMB1; this effect was stronger in a subgroup of affected male sibling pair families, implying a possible specific sex-related effect for this variant. 15523497 2005
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 GeneticVariation disease BEFREE Analysis of genetic variants provided evidence for association with autism for one of the new missense changes identified in LAMB1; this effect was stronger in a subgroup of affected male sibling pair families, implying a possible specific sex-related effect for this variant. 15523497 2005
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.330 Biomarker disease BEFREE Four candidate genes (NRCAM, LRRN3, KIAA0716, and LAMB1) in this region were chosen for examination based on their proximity to the marker most consistently cosegregating with autism in these families (D7S1817), their tissue expression patterns, and likely biological relevance to autism. 15128462 2004