- abnormal hair follicle morphology / MGI
- distorted hair follicle pattern / MGI
- sparse hair / MGI
- delayed hair appearance / MGI
- small spleen / MGI
- abnormal Peyer's patch morphology / MGI
- abnormal epidermal layer morphology / MGI
- hyperkeratosis / MGI
- decreased body weight / MGI
- hyperactivity / MGI
- postnatal growth retardation / MGI
- abnormal homeostasis / MGI
- decreased IgM level / MGI
- abnormal B cell differentiation / MGI
- decreased spleen weight / MGI
- decreased B cell number / MGI
- abnormal amino acid level / MGI
- abnormal enzyme/coenzyme activity / MGI
- decreased Peyer's patch number / MGI
- small Peyer's patches / MGI
- decreased transitional stage B cell number / MGI
- decreased pre-B cell number / MGI
- abnormal spleen B cell follicle morphology / MGI
- abnormal enterocyte physiology / MGI
- decreased skeletal muscle fiber diameter / MGI
- abnormal blood homeostasis / MGI
FVB-Tg(Fabp2-Arg1)1Wla/Cnbc
Status | Available to order |
EMMA ID | EM:05159 |
Citation information | RRID:IMSR_EM:05159 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 | FVB-Tg(Fabp2-Arg1)1Wla/Cnbc |
Alternative name | FA/2 FVB |
Strain type | Transgenic Strains |
Allele/Transgene symbol | Tg(Fabp2-Arg1)1Wla |
Gene/Transgene symbol | Tg(Fabp2-Arg1)1Wla |
Information from provider
Provider | Wouter Lamers |
Provider affiliation | Maastricht University |
Genetic information | Transgenic mouse line that overexpresses arginase I in the enterocytes only (cDNA of rat arginase 1 under control of FABPi promoter). |
Phenotypic information | The phenotype of suckling F/A2 mice (hypoargininemia, reduced hair and muscle growth, impaired B-cell maturation, impaired pituitary growth-hormone secretion, and decreased liver Igf1 mRNA production and plasma IGF1 concentration) results from activation of the general control non-derepressible 2 (GCN2) stress kinase signaling pathway, without impacting mTORC1-mediated signaling. |
Breeding history | Backcrossed more than 10 times to C57BL/6J, bred as heterozygote versus wild type. |
References |
|
Homozygous fertile | no |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous FVB/N males, wild-type FVB/N females |
Stage of embryos | 8-cell |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal hair follicle morphology / MGI
- distorted hair follicle pattern / MGI
- sparse hair / MGI
- delayed hair appearance / MGI
- small spleen / MGI
- abnormal Peyer's patch morphology / MGI
- abnormal epidermal layer morphology / MGI
- hyperkeratosis / MGI
- decreased body weight / MGI
- hyperactivity / MGI
- postnatal growth retardation / MGI
- decreased IgM level / MGI
- abnormal B cell differentiation / MGI
- decreased spleen weight / MGI
- decreased B cell number / MGI
- abnormal amino acid level / MGI
- abnormal enzyme/coenzyme activity / MGI
- decreased Peyer's patch number / MGI
- small Peyer's patches / MGI
- decreased transitional stage B cell number / MGI
- decreased pre-B cell number / MGI
- abnormal spleen B cell follicle morphology / MGI
- abnormal enterocyte physiology / MGI
- decreased skeletal muscle fiber diameter / MGI
- increased ornithine level / MGI
- increased circulating glycine level / MGI
- decreased circulating arginine level / MGI
- decreased arginine level / MGI
Literature references
- Effect of arginine deficiency on arginine-dependent post-translational protein modifications in mice.;Kwikkers Karin L, Ruijter Jan M, Labruyère Wil T, McMahon Kathryn K, Lamers Wouter H, ;2005;The British journal of nutrition;93;183-9; 15788111
- Arginine deficiency affects early B cell maturation and lymphoid organ development in transgenic mice.;de Jonge Wouter J, Kwikkers Karin L, te Velde Anje A, van Deventer Sander J H, Nolte Martijn A, Mebius Reina E, Ruijter Jan M, Lamers Marinus C, Lamers Wouter H, ;2002;The Journal of clinical investigation;110;1539-48; 12438451
- Overexpression of arginase I in enterocytes of transgenic mice elicits a selective arginine deficiency and affects skin, muscle, and lymphoid development.;de Jonge Wouter J, Hallemeesch Marcella M, Kwikkers Karin L, Ruijter Jan M, de Gier-de Vries Corrie, van Roon Marian A, Meijer Alfred J, Marescau Bart, de Deyn Peter P, Deutz Nicolaas E P, Lamers Wouter H, ;2002;The American journal of clinical nutrition;76;128-40; 12081826
- Overexpression of arginase alters circulating and tissue amino acids and guanidino compounds and affects neuromotor behavior in mice.;de Jonge W J, Marescau B, D'Hooge R, De Deyn P P, Hallemeesch M M, Deutz N E, Ruijter J M, Lamers W H, ;2001;The Journal of nutrition;131;2732-40; 11584097
- Arginine deficiency causes runting in the suckling period by selectively activating the stress kinase GCN2.;Marion Vincent, Sankaranarayanan Selvakumari, de Theije Chiel, van Dijk Paul, Lindsey Patrick, Lamers Marinus C, Harding Heather P, Ron David, Lamers Wouter H, Köhler S Eleonore, ;2011;The Journal of biological chemistry;286;8866-74; 21239484
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