- decreased circulating HDL cholesterol level / IMPC
- tremors / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- abnormal bone structure / IMPC
- increased lean body mass / IMPC
- decreased circulating cholesterol level / IMPC
- impaired glucose tolerance / IMPC
- increased circulating aspartate transaminase level / IMPC
- decreased circulating serum albumin level / IMPC
- decreased circulating total protein level / IMPC
- decreased pulmonary respiratory rate / IMPC
- increased circulating amylase level / IMPC
- decreased total body fat amount / IMPC
- decreased grip strength / IMPC
- decreased fasting circulating glucose level / IMPC
C57BL/6N-Nrxn1tm1b(KOMP)Wtsi/H
| Status | Only small colony available |
| EMMA ID | EM:16263 |
| Citation information | RRID:IMSR_EM:16263 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| International strain name | C57BL/6N-Nrxn1tm1b(KOMP)Wtsi/H |
| Alternative name | EPD0796_5_E08 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Nrxn1tm1b(KOMP)Wtsi |
| Gene/Transgene symbol | Nrxn1 |
| Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
| Provider | Mary Lyon Centre at MRC Harwell |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This mouse line originates from KOMP ES clone EPD0796_5_E08. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele. Click here for more information on KOMP final vectors. |
| Phenotypic information | Potential phenotyping data in the IMPC portal |
| References | None available |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Pitt-Hopkins-like syndrome / Orphanet_221150
- NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance / Orphanet_600663
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal bone structure / IMPC
- tremors / IMPC
- increased circulating amylase level / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- decreased grip strength / IMPC
- decreased pulmonary respiratory rate / IMPC
- decreased circulating cholesterol level / IMPC
- decreased total body fat amount / IMPC
- decreased circulating total protein level / IMPC
- decreased circulating serum albumin level / IMPC
- impaired glucose tolerance / IMPC
- decreased fasting circulating glucose level / IMPC
- decreased circulating HDL cholesterol level / IMPC
- increased lean body mass / IMPC
- increased circulating aspartate transaminase level / IMPC
MGI phenotypes (gene matching)
- increased grooming behavior / MGI
- abnormal nest building behavior / MGI
- no abnormal phenotype detected / MGI
- abnormal motor learning / MGI
- abnormal excitatory postsynaptic currents / MGI
- abnormal nervous system physiology / MGI
- decreased synaptic glutamate release / MGI
- abnormal miniature excitatory postsynaptic currents / MGI
- behavior/neurological phenotype / MGI
- decreased prepulse inhibition / MGI
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