- hydronephrosis / MGI
- abnormal kidney cortex morphology / MGI
- abnormal kidney blood vessel morphology / MGI
- decreased body weight / MGI
- decreased body size / MGI
- hyperactivity / MGI
- polydipsia / MGI
- hypotension / MGI
- polyuria / MGI
- abnormal postnatal growth/weight/body size / MGI
- abnormal kidney morphology / MGI
- decreased circulating aldosterone level / MGI
- dilated renal tubules / MGI
- abnormal juxtaglomerular apparatus morphology / MGI
- decreased heart weight / MGI
- increased systemic arterial blood pressure / MGI
- decreased systemic arterial blood pressure / MGI
- decreased urine osmolality / MGI
- renal interstitial fibrosis / MGI
- increased circulating renin level / MGI
- decreased ovulation rate / MGI
- decreased liver weight / MGI
- increased kidney weight / MGI
- decreased renal glomerulus number / MGI
- dilated kidney collecting duct / MGI
- kidney atrophy / MGI
- abnormal blood-brain barrier function / MGI
- abnormal enzyme/coenzyme level / MGI
- abnormal renal glomerulus morphology / MGI
- renal/urinary system phenotype / MGI
- cardiovascular system phenotype / MGI
- reproductive system phenotype / MGI
- vascular smooth muscle hyperplasia / MGI
- abnormal renal/urinary system physiology / MGI
- increased renal plasma flow rate / MGI
- increased circulating creatinine level / MGI
- abnormal renal filtration rate / MGI
- decreased creatinine clearance / MGI
- increased circulating antidiuretic hormone level / MGI
- decreased urine potassium level / MGI
- decreased systemic arterial diastolic blood pressure / MGI
- decreased systemic arterial systolic blood pressure / MGI
- decreased urine sodium level / MGI
- increased circulating angiotensinogen level / MGI
- decreased circulating angiotensinogen level / MGI
- abnormal hippocampus granule cell layer / MGI
- slow postnatal weight gain / MGI
- decreased fat cell size / MGI
- decreased epididymal fat pad weight / MGI
- abnormal blood homeostasis / MGI
- decreased total body fat amount / MGI
- postnatal lethality, incomplete penetrance / MGI
- kidney papillary atrophy / MGI
- abnormal kidney afferent arteriole morphology / MGI
- abnormal kidney cortex artery morphology / MGI
- abnormal kidney interlobular artery morphology / MGI
- abnormal kidney inner medulla morphology / MGI
- renal tubule atrophy / MGI
- expanded mesangial matrix / MGI
- tubulointerstitial nephritis / MGI
- kidney medulla atrophy / MGI
- kidney cortex atrophy / MGI
- increased urine flow rate / MGI
- decreased urine aldosterone level / MGI
- increased urine antidiuretic hormone level / MGI
- kidney papillary hypoplasia / MGI
- increased fluid intake / MGI
C57BL/6NTac-Agtem1(IMPC)H/H
Status | Available to order |
EMMA ID | EM:14999 |
Citation information | RRID:IMSR_EM:14999 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-Agtem1(IMPC)H/H |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Agtem1(IMPC)H |
Gene/Transgene symbol | Agt |
Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project 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
- Primary hyperoxaluria type 1 / Orphanet_93598
- Renal tubular dysgenesis of genetic origin / Orphanet_97369
MGI phenotypes (gene matching)