NLGN4X

neuroligin 4, X-linked
OMIM: 300427, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green NLGN4X in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.198	review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Expert list Phenotypes Intellectual developmental disorder, X-linked - MIM#300495
Green NLGN4X in Mendeliome Version 1.1891	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Mental retardation, X-linked, MIM# 300495
Green NLGN4X 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 Mental retardation, X-linked, MIM# 300495
Green NLGN4X in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Mackenzie's Mission Phenotypes Mental retardation, X-linked, 300495 (3)
Red NLGN4X in Additional findings_Paediatric Level 2: Screening Version 0.278	review	Unknown	Sources Expert Review Red BabySeq Category C gene Phenotypes Autism
Red NLGN4X in Prepair 1000+ Level 2: Screening Version 1.9	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red Mackenzie's Mission Phenotypes Intellectual developmental disorder, X-linked (MIM#300495)
Red NLGN4X in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red BabySeq Category C gene Phenotypes Intellectual developmental disorder, X-linked MIM#300495