NLGN3

neuroligin 3
OMIM: 300336, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green NLGN3 in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.198	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes X-linked complex neurodevelopmental disorder MONDO:0100148 {Asperger syndrome susceptibility, X-linked 1} - MIM#300494 {Autism susceptibility, X-linked 1} - MIM#300425
Green NLGN3 in Mendeliome Version 1.1902	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes X-linked complex neurodevelopmental disorder MONDO:0100148 {Asperger syndrome susceptibility, X-linked 1} - MIM#300494 {Autism susceptibility, X-linked 1} - MIM#300425
Green NLGN3 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Genetic Health Queensland Phenotypes X-linked complex neurodevelopmental disorder MONDO:0100148 {Asperger syndrome susceptibility, X-linked 1} - MIM#300494 {Autism susceptibility, X-linked 1} - MIM#300425
Red NLGN3 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	Unknown	Sources Expert Review Red BabySeq Category C gene Phenotypes Autism
Red NLGN3 in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	Unknown	Sources BabySeq Category C gene Expert Review Red Phenotypes Autism