- 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
STOCK Scnn1gtm1.1Hum/Orl
| Status | Available to order |
| EMMA ID | EM:04400 |
| Citation information | RRID:IMSR_EM:04400 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 | STOCK Scnn1gtm1.1Hum/Orl |
| Alternative name | Scnn1g lox/lox |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Scnn1gtm1.1Hum |
| Gene/Transgene symbol | Scnn1g |
Information from provider
| Provider | Edith Hummler |
| Provider affiliation | Pharmacology & Toxicology, University of Lausanne |
| Genetic information | An frt-flanked neo cassette with a 3' loxP site was inserted upstream of exon 2, and an additional loxP site was inserted downstream of exon 2. Germ line, flp-recombination was used to remove the neo cassette. |
| Phenotypic information | No phenotype. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
| Animals used for archiving | homozygous males, wild-type C57BL/6N females |
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)
Literature references
- Conditional gene targeting of the ENaC subunit genes Scnn1b and Scnn1g.;Mérillat Anne-Marie, Charles Roch-Philippe, Porret Andrée, Maillard Marc, Rossier Bernard, Beermann Friedrich, Hummler Edith, ;2009;American journal of physiology. Renal physiology;296;F249-56; 19036848
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).
