- increased thigmotaxis / IMPC
- decreased bone mineral density / IMPC
- female infertility / IMPC
- male infertility / IMPC
- improved glucose tolerance / IMPC
- decreased grip strength / IMPC
- increased fasting circulating glucose level / IMPC
- limb grasping / IMPC
- increased urine microalbumin level / IMPC
- decreased locomotor activity / IMPC
- abnormal lens morphology / IMPC
- decreased bone mineral content / IMPC
B6.129S7(Cg)-Syce1tm1Hgu/H
| Status | Available to order |
| EMMA ID | EM:04538 |
| Citation information | RRID:IMSR_EM:04538 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 | B6.129S7(Cg)-Syce1tm1Hgu/H |
| Alternative name | Syce1KO /C57Bl6 |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Syce1tm1Hgu |
| Gene/Transgene symbol | Syce1 |
Information from provider
| Provider | Howard Cooke |
| Provider affiliation | Department of Medical & Developmental Genetics, MRC Human Genetics Unit |
| Genetic information | Exons 2 through 11 were replaced with an IRES/lacZ and floxed neo cassette. |
| Phenotypic information | Mice homozygous for this mutation in this background can not progress to diplotene stages of meiosis and show a failure of synapsis. Heterozygous mice show close to normal fertility. |
| Breeding history | Founder males were initially crossed onto CD1 outbred females. Subsequently males were backcrossed 8 generations to C57BL/6J. |
| References |
|
| Homozygous fertile | no |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
| Animals used for archiving | heterozygous C57BL/6J males |
| Breeding at archiving centre | None. Males were archived at the time of arrival at the archiving centre. |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Male infertility with azoospermia or oligozoospermia due to single gene mutation / Orphanet_399805
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
Literature references
- Mutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repair.;Bolcun-Filas Ewelina, Hall Emma, Speed Robert, Taggart Mary, Grey Corinne, de Massy Bernard, Benavente Ricardo, Cooke Howard J, ;2009;PLoS genetics;5;e1000393; 19247432
Information on how we integrate external resources can be found here
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