- increased white adipose tissue amount / MGI
- myoclonus / MGI
- tremors / MGI
- thin diaphragm muscle / MGI
- abnormal cerebral cortex morphology / MGI
- convulsive seizures / MGI
- abnormal skin condition / MGI
- increased body weight / MGI
- decreased body weight / MGI
- decreased body size / MGI
- delayed eyelid opening / MGI
- increased anxiety-related response / MGI
- abnormal locomotor behavior / MGI
- ataxia / MGI
- hyperactivity / MGI
- hypoactivity / MGI
- no spontaneous movement / MGI
- impaired coordination / MGI
- abnormal object recognition memory / MGI
- abnormal spatial learning / MGI
- unresponsive to tactile stimuli / MGI
- disheveled coat / MGI
- increased circulating triglyceride level / MGI
- hyperglycemia / MGI
- abnormal blood vessel morphology / MGI
- decreased embryo size / MGI
- abnormal dopamine level / MGI
- infertility / MGI
- respiratory failure / MGI
- seizures / MGI
- abnormal motor capabilities/coordination/movement / MGI
- increased circulating insulin level / MGI
- premature death / MGI
- abnormal brain morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal CNS synaptic transmission / MGI
- abnormal intercostal muscle morphology / MGI
- hepatic steatosis / MGI
- akinesia / MGI
- decreased glucagon secretion / MGI
- decreased vertical activity / MGI
- increased thigmotaxis / MGI
- blotchy skin / MGI
- abnormal PNS synaptic transmission / MGI
- abnormal endplate potential / MGI
- enhanced paired-pulse facilitation / MGI
- decreased paired-pulse facilitation / MGI
- no phenotypic analysis / MGI
- decreased insulin secretion / MGI
- decreased width of hypertrophic chondrocyte zone / MGI
- abnormal pancreatic beta cell physiology / MGI
- abnormal insulin secretion / MGI
- decreased synaptic glutamate release / MGI
- abnormal miniature excitatory postsynaptic currents / MGI
- increased circulating cholesterol level / MGI
- improved glucose tolerance / MGI
- abnormal serotonin level / MGI
- insulin resistance / MGI
- behavior/neurological phenotype / MGI
- taste/olfaction phenotype / MGI
- increased susceptibility to diet-induced obesity / MGI
- increased circulating leptin level / MGI
- increased body mass index / MGI
- impaired hearing / MGI
- abnormal hippocampus CA3 region morphology / MGI
- increased white fat cell size / MGI
- decreased prepulse inhibition / MGI
- abnormal impulsive behavior control / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, complete penetrance / MGI
- decreased circulating ghrelin level / MGI
- increased food intake / MGI
- decreased food intake / MGI
C57BL/6NCrl-Snap25em1(IMPC)Ccpcz/Ph
| Status | Under development - register interest |
| EMMA ID | EM:16682 |
| Citation information | RRID:IMSR_EM:16682 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/6NCrl-Snap25em1(IMPC)Ccpcz/Ph |
| Alternative name | |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Snap25em1(IMPC)Ccpcz |
| Gene/Transgene symbol | Snap25 |
Information from provider
| Provider | Institute of Molecular Genetics |
| Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
| Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
| Phenotypic information | Potential phenotyping data in the IMPC portal |
| References | None available |
Information from EMMA
| Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Presynaptic congenital myasthenic syndromes / Orphanet_98914
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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