- 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
C57BL/6N-Eps8l2tm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:10398 |
International strain name | C57BL/6N-Eps8l2tm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0679_3_D06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Eps8l2tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Eps8l2 |
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 EPD0679_3_D06. 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)
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