- decreased bone mineral density / IMPC
- decreased locomotor activity / IMPC
- increased circulating alkaline phosphatase level / IMPC
- decreased grip strength / IMPC
- decreased circulating chloride level / IMPC
- increased circulating cholesterol level / IMPC
- decreased bone mineral content / IMPC
- increased neutrophil cell number / IMPC
- increased lean body mass / IMPC
- impaired glucose tolerance / IMPC
- increased circulating HDL cholesterol level / IMPC
- increased circulating amylase level / IMPC
- decreased total body fat amount / IMPC
- decreased exploration in new environment / IMPC
- increased circulating creatinine level / IMPC
- increased circulating total protein level / IMPC
C57BL/6NTac-Aqp1tm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:09371 |
Citation information | RRID:IMSR_EM:09371 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/6NTac-Aqp1tm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0508_2_C01 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Aqp1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Aqp1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
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 EPD0508_2_C01. 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
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased body weight / MGI
- dehydration / MGI
- postnatal growth retardation / MGI
- abnormal respiratory system physiology / MGI
- decreased urine osmolality / MGI
- decreased vascular permeability / MGI
- nervous system phenotype / MGI
- abnormal myocardial fiber physiology / MGI
- lethargy / MGI
- hearing/vestibular/ear phenotype / MGI
- endocrine/exocrine gland phenotype / MGI
- behavior/neurological phenotype / MGI
- vision/eye phenotype / MGI
- decreased urine sodium level / MGI
- dilated rete testis / MGI
- increased blood osmolality / MGI
- prenatal lethality, incomplete penetrance / MGI
- abnormal renal water transport / MGI
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).