- 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
C57BL/6N-Adcy1tm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:08506 |
Citation information | RRID:IMSR_EM:08506 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-Adcy1tm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0846_1_B05 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Adcy1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Adcy1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | MRC, Medical Research Council |
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. |
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 (gene matching)
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
Information on how we integrate external resources can be found here
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