- decreased body length / IMPC
- decreased bone mineral content / IMPC
- decreased prepulse inhibition / IMPC
- decreased bone mineral density / IMPC
- decreased lean body mass / IMPC
- decreased locomotor activity / IMPC
- decreased thigmotaxis / IMPC
- increased total body fat amount / IMPC
- increased fasting circulating glucose level / IMPC
- decreased total retina thickness / IMPC
- impaired glucose tolerance / IMPC
- abnormal retina inner nuclear layer morphology / IMPC
129-Iqsec3tm1(IRES-lacZ-neo)Wtsi/WtsiH
| Status | Available to order |
| EMMA ID | EM:15825 |
| Citation information | RRID:IMSR_EM:15825 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 | 129-Iqsec3tm1(IRES-lacZ-neo)Wtsi/WtsiH |
| Alternative name | 129-Iqsec3 |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Iqsec3tm1(IRES-lacZ-neo)Wtsi |
| Gene/Transgene symbol | Iqsec3 |
Information from provider
| Provider | Seth Grant |
| Provider affiliation | Wellcome Trust Sanger Institute |
| Genetic information | Information sourced from supplementary data 1 for dhttps://doi.org/10.1101/500389: This knockout mouse strain was created via ES cells to mouse conversion. E14TG2a ES cells were targeted with a vector which replaced This replaced 3kb of Iqsec3 genomic DNA (X121360567 to X121363526; Ensemble Build 55) with IRES-lacZ-neo cassette in exon 4-5 leading to a frameshift mutation between exon 3 and 6. |
| Phenotypic information | Mutant mice showed medium overall behavioural difference from wildtypes, with eight of 16 behaviour variables significantly impacted in these mutant mice. In the elevated plus maze task, four behavioural variables of five were significantly impacted in mutants. In the open field/novel object exploration task, one behavioural variable, OF NOE total distance, was significantly increased in mutants. In the fear learning task, two behavioural variables of two were significantly impacted in mutants. In the contextual memory task, one behavioural variable, contextual memory mean, was significantly decreased in mutants. Only rotarod and cued memory tasks were unaffected. |
| Breeding history | Mice were maintained by backcrossing onto the 129S5/ SvEvBrd background; heterozygous males and females were fertile and used to set up intercrosses to generate homozygous and wildtype mice to study. |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | yes |
| Homozygous matings required | not known |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (gene matching)
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).
