- spleen hypoplasia / MGI
- small testis / MGI
- postnatal growth retardation / MGI
- thymus hypoplasia / MGI
- reduced female fertility / MGI
- male infertility / MGI
- delayed vaginal opening / MGI
- small uterus / MGI
- homeostasis/metabolism phenotype / MGI
- hematopoietic system phenotype / MGI
- postnatal lethality, incomplete penetrance / MGI
B6.129P2-Sp4tm1Sus/Cnrm
Status | Available to order |
EMMA ID | EM:02431 |
Citation information | RRID:IMSR_EM:02431 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 | B6.129P2-Sp4tm1Sus/Cnrm |
Alternative name | Sp4 knockout |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Sp4tm1Sus |
Gene/Transgene symbol | Sp4 |
Information from provider
Provider | Sjaak Philipsen |
Provider affiliation | Genetics, Erasmus MC |
Genetic information | A targeting vector was designed to replace sequences that encode the N-terminal activation domains of Sp4 protein (amino acids 4-557). This was obtained by replacing exons 2 and 3 of the mouse Sp4 gene by IRES-LacZ-polyA/PGK-neo sequences in the targeting vector. The lacZ gene is expressed under control of the endogenous Sp4 promoter. |
Phenotypic information | Increased mortality in the first weeks after birth, possibly due to cardiac arrest. Infertile; the animals are not interested in reproductive activities. Heterozygote Sp4 knockouts have no known phenotype. |
Breeding history | The line was backcrossed to C57BL/6 for more than 20 generations. |
References |
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Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- spleen hypoplasia / MGI
- abnormal hippocampus morphology / MGI
- abnormal dentate gyrus morphology / MGI
- small testis / MGI
- decreased body size / MGI
- reduced male mating frequency / MGI
- abnormal locomotor behavior / MGI
- hyperactivity / MGI
- impaired coordination / MGI
- decreased exploration in new environment / MGI
- reduced long term potentiation / MGI
- abnormal startle reflex / MGI
- irregular heartbeat / MGI
- postnatal growth retardation / MGI
- thymus hypoplasia / MGI
- reduced female fertility / MGI
- male infertility / MGI
- premature death / MGI
- gliosis / MGI
- reduced sensorimotor gating / MGI
- delayed vaginal opening / MGI
- small uterus / MGI
- decreased vertical activity / MGI
- abnormal impulse conducting system conduction / MGI
- nervous system phenotype / MGI
- impaired passive avoidance behavior / MGI
- abnormal heartbeat / MGI
- absent heartbeat / MGI
- abnormal Purkinje fiber morphology / MGI
- homeostasis/metabolism phenotype / MGI
- endocrine/exocrine gland phenotype / MGI
- cardiovascular system phenotype / MGI
- reproductive system phenotype / MGI
- hematopoietic system phenotype / MGI
- abnormal spatial reference memory / MGI
- slow postnatal weight gain / MGI
- ventricular tachycardia / MGI
- impaired contextual conditioning behavior / MGI
- impaired cued conditioning behavior / MGI
- ventricular premature beat / MGI
- atrioventricular block / MGI
- sinoatrial block / MGI
- sinus bradycardia / MGI
- postnatal lethality, incomplete penetrance / MGI
- perinatal lethality, incomplete penetrance / MGI
- impaired spatial learning / MGI
Literature references
- Complex phenotype of mice homozygous for a null mutation in the Sp4 transcription factor gene.;Göllner H, Bouwman P, Mangold M, Karis A, Braun H, Rohner I, Del Rey A, Besedovsky H O, Meinhardt A, van den Broek M, Cutforth T, Grosveld F, Philipsen S, Suske G, ;2001;Genes to cells : devoted to molecular & cellular mechanisms;6;689-97; 11532028
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