- weight loss / MGI
- no abnormal phenotype detected / MGI
- oliguria / MGI
- pallor / MGI
- lethargy / MGI
- decreased urine potassium level / MGI
- increased circulating potassium level / MGI
- decreased circulating sodium level / MGI
- increased urine sodium level / MGI
- postnatal lethality, incomplete penetrance / MGI
- increased wet-to-dry lung weight ratio / MGI
- increased urine bicarbonate level / MGI
- decreased respiratory epithelial sodium ion transmembrane transport / MGI
- decreased intestinal epithelial sodium ion transmembrane transport / MGI
C57BL/6N-Scnn1gtm1e(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:07574 |
International strain name | C57BL/6N-Scnn1gtm1e(EUCOMM)Wtsi/H |
Alternative name | EPD0795_5_H04 |
Strain type | Targeted Mutant Strains : Targeted Non-conditional |
Allele/Transgene symbol | Scnn1gtm1e(EUCOMM)Wtsi |
Gene/Transgene symbol | Scnn1g |
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 EPD0795_5_H04. For further details on the construction of this clone see the page at the IMPC portal. The targeted allele has lost the 3' loxP site. These mutations cannot be converted into conditional alleles. 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
- Generalized pseudohypoaldosteronism type 1 / Orphanet_171876
- Liddle syndrome / Orphanet_526
- Idiopathic bronchiectasis / Orphanet_60033
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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