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Symbol Name ID |
Nrxn1
neurexin I MGI:1096391 |
| Darker colors indicate more annotations |
| Human Phenotypes | Drooling |
Intellectual disability, severe |
Broad-based gait |
Epileptic encephalopathy |
Developmental regression |
| Disease(s) Associated with NRXN1 | |||||
| Pitt-Hopkins-like syndrome 2 |
| Mouse Phenotypes | abnormal nervous system physiology |
abnormal excitatory postsynaptic currents |
abnormal miniature excitatory postsynaptic currents |
decreased prepulse inhibition |
decreased synaptic glutamate release |
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| Availability | Mouse Genotype | |||||
| Nrxn1tm1Sud/Nrxn1tm1Sud | ||||||
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 04/23/2024 MGI 6.23 |
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