- abnormal coat appearance / IMPC
- decreased total retina thickness / IMPC
- abnormal bone structure / IMPC
- irregularly shaped pupil / IMPC
- decreased prepulse inhibition / IMPC
- increased heart rate / IMPC
- increased bone mineral content / IMPC
- abnormal retina blood vessel morphology / IMPC
- abnormal retina outer nuclear layer morphology / IMPC
- abnormal eye anterior chamber depth / IMPC
- hyperactivity / IMPC
- increased vertical activity / IMPC
- abnormal eye posterior chamber depth / IMPC
C57BL/6-Slc44a1em1Cnbc/Cncb
| Status | Available to order |
| EMMA ID | EM:15672 |
| Citation information | RRID:IMSR_EM:15672 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/6-Slc44a1em1Cnbc/Cncb |
| Alternative name | Slc44a1( KO exon 2) |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Slc44a1em1Cnbc |
| Gene/Transgene symbol | Slc44a1 |
Information from provider
| Provider | Ekaitz Errasti Murugarren |
| Provider affiliation | Department of Physiological Sciences, , School of Medicine, University of Barcelona |
| Genetic information | The Slc44a1 mouse line was created using CRISPR/Cas9 technology, p.Arg15Glndelfsx34: deletion of 1 bp in exon 2, generating a truncated protein from amino acid 15 (arginine). These mice express the Arg15Glndelfsx34 protein in the Slc44a1 gene. CRISPR technology details: The mouse model was generated using Cas9 protein and guide RNA (crRNA+tracrRNA) and therefore the coding sequence for Cas9 has not been integrated in the mouse genome. |
| Phenotypic information | Homozygous:UnknownHeterozygous:Unknown |
| Breeding history | The mouse line was generated in C57BL/6 genetic background. Less than 10 generations. |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Disease and phenotype information
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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