NRXN1

neurexin 1
OMIM: 600565, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green NRXN1 in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.198	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Pitt-Hopkins-like syndrome 2 - MIM#614325
Green NRXN1 in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Pitt-Hopkins-like syndrome 2 - MIM#614325
Green NRXN1 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.33 Component of the following Super Panels: Progressive Neurological Conditions	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Australian Genomics Health Alliance Epilepsy Flagship Phenotypes Pitt-Hopkins-like syndrome 2 - MIM#614325
Green NRXN1 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Pitt-Hopkins-like syndrome 2 - MIM#614325
Red NRXN1 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	Unknown	Sources Expert Review Red BabySeq Category C gene Phenotypes Autism
Red NRXN1 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	Unknown	Sources BabySeq Category C gene Expert Review Red Phenotypes Autism