- increased leukocyte cell number / IMPC
- abnormal locomotor behavior / IMPC
- hyperactivity / IMPC
- abnormal gait / IMPC
- increased exploration in new environment / IMPC
- increased circulating phosphate level / IMPC
- abnormal coat/hair pigmentation / IMPC
- increased mean corpuscular volume / IMPC
- improved glucose tolerance / IMPC
- increased circulating creatine kinase level / IMPC
C57BL/6N-Adcy1tm1b(EUCOMM)Wtsi/H
| Status | Only small colony available |
| EMMA ID | EM:16856 |
| Citation information | RRID:IMSR_EM:16856 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-Adcy1tm1b(EUCOMM)Wtsi/H |
| Alternative name | EPD0846_1_B05 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Adcy1tm1b(EUCOMM)Wtsi |
| Gene/Transgene symbol | Adcy1 |
| 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 EUCOMM ES clone EPD0846_1_B05. 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 EUCOMM 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
- Autosomal recessive non-syndromic sensorineural deafness type DFNB / Orphanet_90636
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- hyperactivity / IMPC
- abnormal coat/hair pigmentation / IMPC
- increased exploration in new environment / IMPC
- increased circulating creatine kinase level / IMPC
- increased mean corpuscular volume / IMPC
- improved glucose tolerance / IMPC
- abnormal locomotor behavior / IMPC
- increased circulating phosphate level / IMPC
- abnormal gait / IMPC
- increased leukocyte cell number / IMPC
MGI phenotypes (gene matching)
- abnormal thalamus morphology / MGI
- disorganized barrel cortex / MGI
- absent barrels in primary somatosensory cortex / MGI
- abnormal spatial learning / MGI
- impaired synaptic plasticity / MGI
- abnormal somatosensory cortex physiology / MGI
- abnormal CNS synaptic transmission / MGI
- abnormal excitatory postsynaptic currents / MGI
- abnormal excitatory postsynaptic potential / MGI
- nervous system phenotype / MGI
- hyporesponsive to tactile stimuli / MGI
- abnormal enzyme/coenzyme activity / MGI
- increased chemical nociceptive threshold / MGI
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