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Symbol
Name
ID

Nlgn1
neuroligin 1
MGI:2179435

Phenotype annotations related to nervous system

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

Human Phenotypes	EEG abnormality	Abnormal nonverbal communicative behavior	Delayed speech and language development	Lack of spontaneous play	Impaired ability to form peer relationships	Autism	Inflexible adherence to routines	Motor stereotypy	Restrictive behavior	Intellectual disability	Seizure
Disease(s) Associated with NLGN1
autistic disorder

Mouse Phenotypes		nervous system phenotype	abnormal CNS synaptic transmission	decreased excitatory postsynaptic current amplitude
Availability	Mouse Genotype	nervous system phenotype	abnormal CNS synaptic transmission	decreased excitatory postsynaptic current amplitude
	Nlgn1^em1Taku/Nlgn1^em1Taku	*
	Nlgn1^tm1Bros/Nlgn1^tm1Bros
	Nlgn1^em1Taku/Nlgn1⁺	*
	Tg(Thy1-Nlgn1)6Hnes/0	*
	Nlgn1^tm1.1Sud/Nlgn1^tm1.1Sud Tg(Pcp2-cre)2Mpin/? (conditional)	*

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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