- decreased circulating calcium level / IMPC
- abnormal snout morphology / IMPC
- abnormal startle reflex / IMPC
- decreased startle reflex / IMPC
- abnormal ear morphology / IMPC
- increased circulating alkaline phosphatase level / IMPC
- decreased circulating cholesterol level / IMPC
- increased circulating aspartate transaminase level / IMPC
- increased circulating bilirubin level / IMPC
- decreased circulating serum albumin level / IMPC
- decreased prepulse inhibition / IMPC
- impaired cued conditioning behavior / IMPC
- decreased circulating fructosamine level / IMPC
C57BL/6N-Eps8l2tm1b(EUCOMM)Wtsi/H
| Status | Only small colony available |
| EMMA ID | EM:16238 |
| Citation information | RRID:IMSR_EM:16238 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-Eps8l2tm1b(EUCOMM)Wtsi/H |
| Alternative name | EPD0679_3_D06 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Eps8l2tm1b(EUCOMM)Wtsi |
| Gene/Transgene symbol | Eps8l2 |
| 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 EPD0679_3_D06. 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)
- abnormal startle reflex / IMPC
- increased circulating alkaline phosphatase level / IMPC
- decreased circulating fructosamine level / IMPC
- abnormal ear morphology / IMPC
- decreased circulating serum albumin level / IMPC
- decreased prepulse inhibition / IMPC
- decreased circulating cholesterol level / IMPC
- increased circulating aspartate transaminase level / IMPC
- decreased circulating calcium level / IMPC
- impaired cued conditioning behavior / IMPC
- increased circulating bilirubin level / IMPC
- decreased startle reflex / IMPC
- abnormal snout morphology / IMPC
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).
