Symbol Name ID |
Nlgn1
neuroligin 1 MGI:2179435 |
* | 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 |
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Availability | Mouse Genotype | |||||
Nlgn1em1Taku/Nlgn1em1Taku | * | |||||
Nlgn1em1Taku/Nlgn1+ | * | |||||
Tg(Thy1-Nlgn1)6Hnes/0 | * |
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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last database update 07/05/2024 MGI 6.24 |
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