Symbol Name ID |
Nrxn1
neurexin I MGI:1096391 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties |
Disease(s) Associated with NRXN1 | |
Pitt-Hopkins-like syndrome 2 |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal motor learning |
increased grooming behavior |
tremors |
decreased grip strength |
abnormal nest building behavior |
|
Availability | Mouse Genotype | ||||||
Nrxn1tm1b(KOMP)Wtsi/Nrxn1tm1b(KOMP)Wtsi | |||||||
Nrxn1tm1Sud/Nrxn1tm1Sud | * | ||||||
Nrxn1tm1b(KOMP)Wtsi/Nrxn1+ |
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 08/21/2024 MGI 6.24 |
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