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Symbol
Name
ID

Nlgn1
neuroligin 1
MGI:2179435

Phenotype annotations related to behavior/neurological

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Lack of spontaneous play	Impaired ability to form peer relationships	Autism	Inflexible adherence to routines	Motor stereotypy	Restrictive behavior
Disease(s) Associated with NLGN1
autistic disorder

Mouse Phenotypes		behavior/neurological phenotype	impaired spatial learning	abnormal spatial reference memory	decreased aggression towards mice	abnormal social investigation
Availability	Mouse Genotype	behavior/neurological phenotype	impaired spatial learning	abnormal spatial reference memory	decreased aggression towards mice	abnormal social investigation
	Nlgn1^em1Taku/Nlgn1^em1Taku	*
	Nlgn1^em1Taku/Nlgn1⁺	*
	Tg(Thy1-Nlgn1)6Hnes/0	*

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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